1. HIVtools :: Lipodystrophy Another hypothesis was espoused from a similar metabolic syndrome calledmadelungs disease or multiple symmetric lipomatosis (MSL). http://www.hivtools.com/lipodystrophy.php

Lipid Remodeling Syndrome Hypothesis of Lipid Remodeling Syndrome Antiretroviral Induced Mitochondrial Toxicity Management of NRTI-Induced Mitochondrial Toxicity Lipid Remodeling Syndrome HAART has changed the clinical course of HIV. Patients are no longer dying with overwhelming infections and wasting syndrome. The time to death has also been extended to the point where patients now may have hope of newer developments leading to an eventual cure. This hope has been moderated by new complications such as Lipid Remodeling Syndrome (RMS), which clinically presents as a wasting of the extremities with concomitant central abdominal adiposity. This metabolic abnormality can increase the risk of developing cardiovascular complications such as atherosclerosis, hypertension, and myocardial infarction. Most of the patients who developed RMS were receiving PIs, which were thought to be the cause of this lipid dysregulation. When patients are switched to non-PI containing regimens, resolution of some of the metabolic abnormalities is noted. This gives rise to the hypothesis that HIV-related lipid remodeling is a drug-induced problem. At the present, there is still no consensus or guideline in regards to the definition or the severity of HIV-related lipid remodeling syndrome (RMS). However, most clinicians will agree that patients with peripheral fat wasting (fat loss in the distal extremities, buttock, and face) represent a manifestation of the metabolic disorder. In addition to the peripheral wasting, there is an accumulation of fat in the truncal region, appearing near the dorsocervical area (buffalo hump), breast, and abdominal cavity.

2. AEGiS-BETA: The Wide-Ranging Effects Of Nucleoside Analogs - Summer, 2000 between HAARTassociated lipodystrophy and a form of multiple symmetrical lipomatosis(abnormal fat accumulations), also known as MSL or madelungs disease. http://www.aegis.com/pubs/beta/2000/BE000606.html

Important note: Information in this article was accurate in June 2000. The state of the art may have changed since the publication date. The Wide-Ranging Effects Of Nucleoside Analogs Bulletin of Experimental Treatments for AIDS, Summer, 2000 Dave Gilden September 25, 1999: A group of French doctors report on five cases of a rare syndrome of cerebral, neurologic, and/or retinal damage in 8 of 2,000 babies born to HIV positive mothers. This large mother-child cohort had received AZT (Retrovir) or AZT/3TC (Epivir) to prevent HIV transmission during pregnancy and delivery. The babies also displayed a variety of other abnormalities in muscle, heart, pancreas, and bone marrow activity. Underlying defects in energy production also were apparent. Two of the babies died after about a year. All were HIV negative. October 14, 1999: U.S. Bioscience announces the termination of a trial of their experimental nucleoside analog or nucleoside reverse transcriptase inhibitor (NRTI) lodenosine because of "serious adverse events." On October 11, one of the trial participants died due to a striking liver failure syndrome that continued to worsen for a month after he had stopped taking lodenosine. Three similar deaths occurred in the seven weeks after the remaining trial participants were taken off lodenosine. Another nine persons had to be hospitalized for monitoring and treatment. In all, 75 trial participants exhibited some sign of liver damage in blood tests.

3. Listings Of The World Health Conditions And Diseases Nutrition Listings World Health Conditions and Diseases Nutrition and MetabolismDisorders madelungs disease. Listings World, http://listingsworld.com/Health/Conditions_and_Diseases/Nutrition_and_Metabolism

4. Medweb Question Madelung's Diseasehttp//www.hvmedweb.com/mw1/qanda/madelung%27s_ adjacent entries. madarosis, n. madelungs disease. Madopar, n. Madura foot http://www.hvmedweb.com/mw1/qanda/madelung%27s_disease_medweb.htm

5. Worldbook Medical Encyclopedia > Macula - Ménières Disease > Madura Foot 2. xrefer Madura foot, xrefer - Madura foot adjacent entries. madarosis,n. madelungs disease. Madopar, n. Madura foot . Madurella http://www.s-books.com/wbmedical/32020/32024/Encyclopedias1.htm

Worldbook Medical Encyclopedia Macula - Ménières disease Madura foot Madura foot Search the Web with All Surfable Books World Book Encyclopedia 2000 World Book Medical Encyclopedia Geography History Humanities Industry and Technology Life Science Physical Science and Math Recreation Social Science Documents 1 - 3 of 3 on the subject : Madura foot Public Educational Sources News and Magazines Encyclopedias Madura foot - encyclopedia article from Britannica.com Madura foot - also called Maduromycosis, or Mycetoma, fungus infection, usually localized in the foot but occurring occasionally elsewhere on the body, apparently resulting from inoculation into a scratch or abrasion of any of a number of fungi: Pen http://www.britannica.com/seo/m/madura-foot/ xrefer - Madura foot xrefer - Madura foot ... adjacent entries. madarosis, n. Madelungs disease. Madopar, n. Madura foot . Madurella, n. maduromycosis , n. magenta, n. ... http://www.xrefer.com/entry/126743 xrefer - maduromycosis n. xrefer - maduromycosis n. ... adjacent entries. Madopar, n. Madura foot . Madurella, n. maduromycosis , n. magenta, n. maggot, n. magic bullet. ... http://www.xrefer.com/entry/126745

6. Pathologytoxicology.with1click.com the first dozen or so entries are images of madelungs disease, taken with various scanning techniques. http://pathologytoxicology.with1click.com/

Add Your Site! Headlines Link To Us My History Acronyms Query: "pathology toxicology" Results: 213 Links pathologytoxicology .with1click.com (Use a DRL for your next search!) Is your site listed below? If not, Click Here to add it right away! Next toxicology and pathology services, inc. an independent preclinical toxicology laboratory specializing in classical mammalian systemic toxicology. http://www.toxpath.com/ (Related Links) pathology teaching slide - soft tissue pathology the first dozen or so entries are images of madelungs disease, taken with various scanning techniques. http://www.cuhk.edu.hk/med/paf/slides/soft/soft.htm (Related Links) society of toxicology professional organization of scientists from academic institutions, government, and industry representing scientists who practice toxicology. http://www.toxicology.org (Related Links) toxicology-info.com information on toxicology, drug interactions, toxicity and adverse reactions. part of the altruis biomedical network. http://www.toxicology-info.com/ (Related Links) toxicology sites toxicology sites prepared by dr. hardin.

7. Pathologymicrobiology.with1click.com the first dozen or so entries are images of madelungs disease, taken with various scanning techniques. http://pathologymicrobiology.with1click.com/

Add Your Site! Headlines Link To Us My History Acronyms Query: "pathology microbiology" Results: 301 Links pathologymicrobiology .with1click.com (Use a DRL for your next search!) Is your site listed below? If not, Click Here to add it right away! Next pathology teaching slide - soft tissue pathology the first dozen or so entries are images of madelungs disease, taken with various scanning techniques. http://www.cuhk.edu.hk/med/paf/slides/soft/soft.htm (Related Links) microbiology 310 medical microbiology washington state university - john paznokas http://www.sci.wsu.edu/bio/micro310.html (Related Links) microbiology.com a website for physicians and medical microbiologists. http://www.microbiology.com (Related Links) microbiology develops and transfers basic new technologies and applications in bioprocess engineering, cellular recognition, gene control and expression, and plant and animal molecular biology. http://www.bio.cornell.edu/microbio/sofmicrobio.html (Related Links) 3m microbiology electronic pipettor is a self-calibrating, microprocessor-based system. http://www.3m.com/microbiology/home/products/pipettor/ep over.html

8. Plaintiff Has Dismissed Defendant Larry Casella. As Of The Date Of Plaintiff, Sandra Dallaire, suffers from madelungs disease . which she describes as a genetic condition affecting the http://www.ctd.uscourts.gov/Opinions/021201.GLG.Dallaire.pdf

9. BSL Translate this page BRODIE's disease-madelungs FETTHALS-LAUNOIS BENSAUDE's LIPOMATOSIS-MSLLIPOMATOSI SIMMETRICA BENIGNA Prof. Camillo O. DI CICCO Member http://digilander.libero.it/camdic/LBS.html

LIPOMATOSI SIMMETRICA BENIGNA Prof. Camillo O. DI CICCO Member of " DNA Repair Group " NIH-National Institutes of Health-Bethesda, Maryland XIth Congress of the European Academy of Dermatology and Venereology CASO CLINICO PERSONALE: Da rilevare che, dalla prima descrizione del quadro morboso ad oggi, sono stati pubblicati e documentati nella letteratura scientifica circa 200 casi. IMAGE N 1 IMAGE N 2 IMAGE N 3 DNA BENIGN SYMMETRIC LIPOMATOSIS Prof. Camillo O. DI CICCO Member of " DNA Repair Group " NIH-National Institutes of Health-Bethesda,Maryland XIth Congress of the European Academy of Dermatology and Venereology Subsequently such picture was described from Huguier (1855)), Founder (1863) and Vermeuil (1888). In the years that followed were published several jobs from part of Bucquoy, Dartignolles and Lèjars (1892), Koettnitz (1894), Payr (1895), Lowenthal(1896), Dalchè and Hayem (1897), Preyss (1898). In 1898 with the detailed description of 75 cases clinicians in "De adénolipomatose simmétrique" (Bull.Soc.Mèd.Hop.Paris,Mémoires,1898,1:298-318), P.E. Launois and R. Bensaude defined clearly such rare disease. PERSONAL CLINICAL CASE: To find that, from the first description of the picture today, they have been published and documented in the scientific literature approximately 200 cases.

10. Swedish Version Of Brorson/Fagher Article On Dercum's Disease Or Adiposis Doloro and pain are the most prominent features of the disease, I propose Det bör nämmasatt lipomen vi madelungs syndrom, eller nultipel symmetrisk lipomatos, inte http://dercums_data.tripod.com/bror-swedish.html

Get Five DVDs for $.49 each. Join now. Tell me when this page is updated Note: This may contain some typos - transcription and proofing what I transcribed is not my strong suit Don. LÄKARTIDNINGEN VOLYM/ÅRGÅNG 93 · 10 APRIL 1996 This article is © 1996 by LÄKARTIDENINGEN - The Journal of the Swedish Medical Association DERCUMS SJUKDOM (Dercums disease) Fettvävsreumatism orsakad av immunförsvarsreaktion? Authors: Håkan Brorson, M.D., Ph.D. Department of Plastic and Reconstructive Surgery, Malmö University Hospital, S-205 02 Malmö, Sweden Birger Fagher, M.D., Ph.D. Associate Professor, Department of Internal Medicine, Lund University Hospital, S-221 85 Lund, Sweden Dercums sjukdom, adiposis dolorosa eller, mera allmänt, fettvävsreumatism är en relativt okänd sjukdom trots att den beskrevs redan 1888 av den americakanske neurologen Francis Xavier Dercum. Den drabber företrädesvis 20-40-åriga kvinnor, men kan även debutera hos barn. Kännetecknande är en uttalad smärta i fettväven. Patienterna har liksom fibromyalgikerna ofta nonchalant avfärdats med att "alla feta har lite ont" Sjukdomen är dock klassificerad av WHO. Francis Xavier Dercum föddes i Philadelphia den 10 augusti 1856 under en tid av intensiva politiska konflikter som utmynnade i det amerikanska inbördeskriget. Familjen härstammade ursprungligen från England. Dercums far. Earnest Dercum, var en framgångsrik bokhandlare och spannmålsgrossist, vilket gjorde det möjligt att finansiera sonens studier.

11. 1Up Health > Health Links Directory > Conditions And Diseases: Nutrition And Met DOIA LaunoisBensaude's Lipomatosis A German University site on the disease. Containssome images of the disease (click the images tab at the top of screen). http://www.1uphealth.com/links/nutrition-and-metabolism-disorders-madelungs-dise

Home Contact Us Privacy Caring For Your Well Being Alternative Medicine Clinical Trials Health News Poisons ... Health Topics A-Z Search 1Up Health Health Directory Addictions Alternative Animal ... Weight Loss By Demography Child Health Teen Health Men's Health Women's Health ... Nutrition and Metabolism Disorders : Madelung's Disease Description See Related Categories Health: Conditions and Diseases: Rare Disorders Sites DOIA Launois-Bensaude's Lipomatosis A German University site on the disease. Contains some images of the disease (click the "images" tab at the top of screen). Lipomatosi di Launois-Bensaude (MSL) A site, in both Italian and English, providing a historical perspective of Madelung's Disease. Madelung's Disease: Benign Symmetric Lipomatosis Madelung's disease or Benign Symmetric Lipomatosis is a "sight diagnosis." Only a doctor knowledgeable about the disease can diagnose it. Madelung's Disease, Benign Symmetric Lipomatosis, Multiple Symmetrical Lipomatosis (MSL) or Lanois-Bensaude Syndrome. Describes the symptoms and the problems of diagnosing MSL. Provides additional links and reference information. Madelung's Disease (NORD entry) Briefly describes this rare disorder (also known as Multiple Symmetrical Lipomatosis, Benign Symmetric Lipomatosis or Lanois-Bensaude Syndrome). Also lists two organizations for further reference information. This entry is courtesy of the National Organization for Rare Disorders.

12. Important Lists - PAEDIATRICS, SPINE GENU VARUS Physiological always bilateral. 1. Metabolic bone disease VitD deficiency. madelungs deformity. TORTICOLLIS. may be Congenital or Acquired. http://www.orthoteers.co.uk/Nrujp~ij33lm/Lists-paed_spine.htm

Go Back to SYLLABUS Find in this Page: enter a search term and hit 'enter' (may take a few seconds) Search the Orthoteer Site: Important Lists PAEDIATRICS, SPINE Pes Planus Causes Flexible Physiological Hyperlaxity of ligaments Tib post insufficiency Rigid Peroneal shortening/spasm- due to subtalar irritability Tarsal coalition Idiopathic septic arthritis osteoid osteoma juvenile chronic arthritis traumatic subtalar degenerative change Neuromuscular Muscular imbalance with tight achilles tendon and weak tib post, due to cerebral palsy and spina bifida Other problems which can give the appearance of flat foot Congenital vertical talus Accessory navicular Skew foot Details Pes Cavus Causes Neuromuscular until proven otherwise , as up to 60% found to be neurological Congenital Idiopathic Arthrogryposis Residual CTEV Acquired Neuromuscular Muscular disease eg. Muscular dystrophies Peripheral nerve disease- HSMN Spinal cord problems-Polio, diastematomyelia, tethered cord, syringomyelia, spina bifida Long tract and central disease- Friedrichs ataxia, cerebral palsy Traumatic Compartment syndrome

13. Childhood Upper Extremity Problems madelungs deformity. SHOULDER. Sprengel Shoulder Associated with KlippelFeilsyndrome, kidney disease, scoliosis, and diastematomyelia. http://www.orthoteers.co.uk/Nrujp~ij33lm/Orthpaeduplimb.htm

Go Back to SYLLABUS Find in this Page: enter a search term and hit 'enter' (may take a few seconds) Search the Orthoteer Site: childhood Upper extremity problems EMBRYOLOGY of the Upper Limb Weeks 4 to 6 The upper extremity, with pronated forearms begins to rotate externally. Developmental disturbances during this period gives rise to major congenital malformations. Early suppresion of limb development causes AMELIA (complete abscence of a limb); Late suppression causes MEROMELIA (partial abscence). Weeks 7 to Birth By week 7 the ten finger rays appear and continue to differentiate till week 12 - 13 when the hands appear. The fingers develop as a result of cell death in the tissue between the digits (failure of this causes syndactyly). INTERNATIONAL CLASSIFICATION (FDD.OUC) Failure of Formation Transverse Arrest / Aplasia Amputations: arm, forearm, wrist, hand, digits Longitudinal Arrest Phocomelia: complete, proximal, distal Radial deficiencies ( radial club hand Central deficiencies ( cleft hand Ulnar deficiencies ( ulnar club hand Hypoplastic digits Failure of Differentiation A. Synostosis: elbow, forearm, wrist, metacarpals, phalanges

14. University Orthopaedics Arch. disease Childhood 70362363; Germon TJ, Clarke NMP, Watt I. (1994) Post traumaticlymphocoele. (1993) madelungs deformity masquerading as a bone tumor. http://www.soton.ac.uk/~ortho/pubs_NMPC.htm

University Orthopaedics Mr. N.M.P. Clarke (Consultant Orthopaedic Surgeon and Senior Lecturer) Publications: Roach, H. I. and N. M. P. Clarke . (1999?) Temporary “cell paralysis” as an intermediate stage in the programmed cell death of immature epiphyseal chondrocytes. Bone (submitted) O'Connor,D., Clarke,N.M.P., Hegarty,S.E. and Fairhurst, J.J. (1998)The natural history of popliteal cysts in children: an ultrasound study. The Knee (in print) Roach, H. I., J. E. Baker, and N. M. P. Clarke . (1998) Initiation of the bony epiphysis in long bones: chronology of interactions between the vascular system and the chondrocytes. J. Bone Miner. Res Cox PJA, Clarke NMP. (1997) Improving the outcome of paediatric orthopaedic trauma: an audit of inpatient management in Southampton. Ann. Royal College Surg. Engl. Taylor GR, Clarke NMP. (1997) Monitoring the treatment of developmental dysplasia of the hip with the Pavlik harness - The role of ultrasound. J. Bone Joint Surg. Taylor GR, Gent E, Clarke NMP. (1997) Biepicondylar fracture dislocation of a child's elbow. Injury Craigen MAC, Clarke NMP.

15. Zeldzame Huidziekten G.F1, Inheritance a form is a rare autosomal recessive disease Aetiology unknown symmetricalcircumscribed lipomatosis, Well defined.see also madelungs neck and http://home.tiscali.nl/sb137765/G.L2.html

Leri-Syndrome Alias Age : from childhood onwards Child Adolescent Adult 20 - 40 Inheritance : autosomal dominant gene Symptoms Skin Topography : hands hyperplasia palm plantar Dig1 fbsPrat fibromatosis child Lesch-Nyhan-Syndrome Alias Age : early childhood Inheritance : sex linked recessive gene - Heterozygous females can be detected by doing a tissue culture of fibroblasts.In this culture 2 populations of fibroblasts can be detected and only one cell line wills show the key enzyme. Aetiology metabolic defect -lack of enzyme hypoxanthine - guaninephosphoribosyl transferase - blood uric acid levels are high . Inborn errors metabolism Symptoms Skin Topography : mutilations esp in face lip chin Diagnose DDD : Artefacta Prognosis : There is no explanation for this tendency to self mutilation Letterer-Siwe-Syndrome Alias : see also histiocytosis X Acute disease. Reticulosis nonlipid - Reticulosis acute of infancy - Histiocytosis X acute disseminated Langerhans cell histiocytosis Histiocytosis malignant - Reticulosis histiocytic medullary JAAD 1985 Sept page 522 Holzberg Age : usually in year 2 rare in adults and has been reported in octogenarians.

16. AOA - Training & Examinations 22 Dupuytren's disease. 23 The still hand and the role of the therapist in rehabilitation.24 Developmental diseases absent radius; madelungs deformity http://www.aoa.org.au/trainguide.asp

GUIDE FOR TRAINEES IN ORTHOPAEDIC SURGERY 1. ROYAL AUSTRALASIAN COLLEGE OF SURGEONS GUIDE TO SURGICAL TRAINING 1996 2. DURATION OF ADVANCED TRAINING 3. SUMMARY OF PROGRAMME REQUIREMENTS 4. IN-TRAINING ASSESSMENT - MENTOR ASSESSMENT FORMS ... 16. GUIDELINES - INDUSTRY SPONSORSHIP 1. ROYAL AUSTRALASIAN COLLEGE OF SURGEONS GUIDE TO SURGICAL TRAINING - 1996 All advanced Trainees should read this document carefully. It can be obtained by writing to: Department of Examinations and Training: Royal Australasian College of Surgeons College of Surgeons Gardens Spring Street Melbourne VIC 3000 Reference - Section 18 "Advanced Training in Orthopaedic Surgery" 2. DURATION OF ADVANCED TRAINING Please refer to RACS Guide to Surgical Training 1996 - Section 18, Paragraph 2. "Advanced Training in Orthopaedic Surgery will extend over at least four (4) years of which three (3) years must be spent in one specified training programme. Trainees may spend time in overseas or interstate posts approved by the AOA Director of Training and the Branch Training Committee in each State. In New Zealand these posts are organised by the New Zealand Orthopaedic Association through the Education Committee. It should be pointed out that the minimum period of training is a full four (4) years. If there have been inadequacies in the training due to sickness or other problems the Branch Training Committee in consultation with the Trainee and the Board of Orthopaedic Surgery may ask the Trainee to do a further period of training. Admission to Fellowship will not be approved until the completion of training (Conditional Fellowship may be awarded in the December of the final year of training).

17. Fibrous Dysplasia Support E-Mail Page - MFD Information #3 Donna AL, Australia. Any one know anything about madelungs disease or Mahdeloongz.I am desperate for anything about this disease, Donna is my grandaughter. http://members.cox.net/fdsupport/mfdinfo3.html

E-MAIL PAGE Nancy AC, MD Hi, I am a 49 year old diagnosed with FD at age 9. I am not sure, but believe I may also have MAS; I don't have the cafeaulait spots, but all else. I have had few surguries really and most when I was under the age of 14; one for epiphiseal stapling to control the leg length discrepance and an osteotomy to straighten my left leg. I have had knee surgery as an adult due to osteoarthritis. I have never met another person with FD and so am thrilled to find this website. I walk using 1 or 2 forearm crutches, depending on pain level. I was surprised to see information on the FD reactivating with hormone replacement therapy which I am on. Any info out there? Also I am looking for a new doctor since mine retired, in the Washington DC/Baltimore area. Nancy bottom of page Michael B, CA My son has fibrous dysplasia on his left tibia and has already had one surgery to help correct the deformity. It looks like he will require more surgery and we were wondering where would be the best place to have a second opinion or to have the surgery done. We currently are seeing a pediatric orthopedic doctor out of Children's Hospital of Orange County here in Orange California but are willing to go ANYWHERE for the best treatment possible. If you have any information that would be wonderful! Thank you so much. Shelley Borovinsky (My son Michael is currently 3 years old).

18. Dyschondrosteosis And Madelung Wrist Deformity ( 2002 ) other people and it help's me to understand this very complicated and rare disease. Iam 45 (2002,female) and just diagnosed with bilateral madelungs syndrome. http://www.divdev.fsnet.co.uk/dysch2002.htm

Dyschondrosteosis and Madelung Wrist Deformity ( 2002 ) To return to main MWD / DCS file Personal stories concerning MWD / DCS submitted to this site in year 2002 Start of year 2002 From V in the UK by contact by telephone MWD + DCS Age 51 in 2002 she had a wrist bone removed in 1972 but has had no problems since, doing sport and working with keyboards. There is a family history over 4 generations with MWD and DCS of at least 6 people. One of her daughters has a habit of standing with hands on hips with elbows directly in front so it looks almost as though her head is on back to front. Her mother explained away her own wrist appearance as having been due to falling off a swing as a kid. From S4 in the USA in e-m contact [ CL ] DCS+MWD I just wanted to thank you for the site and all the work you put into it. My attitude towards having MWD has been improved by knowing about others. You are a true blessing! Again thanks! From G in the UK in e-m contact [ CL ] MWD I am an 18 (2002) year-old (female) sufferer of Madelung's Wrist Deformity. I had it diagnosed when I was 15 but suffered symptoms from the age of approx. 11. My consultant at - - - offered no surgical treatment, but I use TENS as well as taking pain-killers usually used to treat arthritis to control the pain. I just wanted to let you know that I thought your web-site was brilliant, because until now I had never heard of anyone else suffering from MWD. It's really helped me to read about other people with similar symptoms to mine, because during the 4 years before I was diagnosed, and even afterwards to a certain extent, I have always felt that people didn't quite believe about my problems. Anyway, thank you so much for putting together the web-site.

19. Dyschondrosteosis And Madelung Wrist Deformity ( 2001 ) friends (I'm now 147 cm), I was then preliminary diagnosed with this disease. willbe very interested in talking to other people who have madelungs and reading http://www.divdev.fsnet.co.uk/dysch2001.htm

Dyschondrosteosis and Madelung Wrist Deformity ( 2001 ) To return to main MWD / DCS file Personal stories concerning MWD / DCS submitted to this site in year 2001 L in Sweden in email contact with [ CL ] DCS+MWD R in UK (also in Hampshire) telephone call only Numerous generations with MWD and DCS in different countries including South Africa. She is participating (2001)with other of her family in genetic testing with a hospital facility in Manchester. In a personal anecdote she referrred to the conditions making it awkward to put on and take off wet suits. No one in her family has pain associated with their form of DCS / MWD C in the Essex,UK in e-mail contact with From M in the UK,currently (2001) [ CL ] MWD followup November 2002 I have just returned from Italy where I saw an expert in genetics who is very familiar with Madelung. He took a blood sample from me and is doing a DNA test of which I do not have the results yet. However the main point is that he said if I was to get pregnant he could do a test to establish whether the baby would be affected by Madelung, in order to enable me to decide whether to carry on with the pregnancy. I appreciate that this is a sensitive topic for many people but I thought it would be useful to those who are thinking of having children and worried about passing on the gene. From S in the USA in e-m contact with [ CL ] MWD From A2 and M in Holland (friends) in e-m contact [ CL ] DCS+MWD From R2 in the UK in e-m contact [ CL ] MWD

20. Pathology Informatics, Inc., Letter M. The Lightning Hypertext of disease. madarosis madcam madcap madd madden maddened maddermadding maddox made madefaction madeira madelung madelungs mader mades5 http://65.222.228.150/letters/m.htm

The Lightning Hypertext of Disease. Letter-by-Letter Word List. Letter M. Baltimore, MD, 1991-2000. Click on any word to launch a search: maa maai maailma maalant ... mzsmncp What is The Lightning Hypertext of Disease? About the Authors Instant Member Registration ($29) via the Internet Slow Member Registration ($29) via Fax Please enter questions or comments in our Guestbook Go directly to Member's Only Page. Random image browser. Even more images! Complete list of words contained in our text , large file (2 Mbytes). Complete list of words contained in our text and the frequencies of their occurrences , large file (3 Mbytes). Other sites: International Foundation for Ethical Research. Johns Hopkins Autopsy Resource. Carnegie Embryological Collection. Pathology Image Search Engine. For additional information, contact Jules Berman at: jjberman1@home.com Last modified: 10/9/2000.

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