21. Open Directory - Health: Conditions And Diseases: D 4); Diptheria@ (6); Dissociative Identity Disorder@ (112); Diverticulitis@(26); dolicocephaly@ (3); Down Syndrome@ (69); Drooling@ (2 http://www.mptdo.com/Health/Conditions_and_Diseases/D/

about dmoz add URL help the entire directory only in Conditions_and_Diseases/D Top Health Conditions and Diseases : D Description A B C D E F G H ... Dystonia Musculorum Deformans Conditions and Diseases " search on: All the Web AltaVista Google USENET Google ... Yahoo Last update: 10:58 PT, Monday, July 8, 2002 - edit bfjrio Angebotsseiten: Reisen erotik

22. D Website Results :: Linkspider UK Identity Disorder@ (107); Diverticulitis@ (26); dolicocephaly@ (3);Down Syndrome@ (74); Drooling@ (2); Dry Eye@ (5); Duane Retraction http://www.linkspider.co.uk/Health/ConditionsandDiseases/D/

D Websites from Linkspider UK Keyword: D Linkspider UK Directory D Search for Directory Tree: Top Health Conditions and Diseases : D (0) Add URL Advertise Here! Personalize Amazon ... Dystonia Musculorum Deformans

23. Katalog :  : Health : Conditions_and_Diseases : D :  - Netz-Tipp.De dolicocephaly (*); Down Syndrome(*); Drooling (*); Dry Eye (*); Duane Retraction Syndrome (*); Dubowitz http://www.netz-tipp.de/kat/Health/Conditions_and_Diseases/D/

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24. Neurological Examination Of Newborns And Infants Much attention should be paid to the head shape dolicocephaly, brachiocephaly,towerlike skull, left or right inclination are all variants of normal skull. http://www.russianadoption.org/Neurologicalexaminationnewbornsandinfants.htm

Neurological examination of newborns and infants Draft translation Central Insitute of improving doctor’s qualification E.A. Edelstein Neurological examination of newborns and infants is based on the same scheme that is used for older children and adults: CN Motor function Reflexes Sensation Meningeal signs It should be noted that neurological status of the newborns has some special features. The mainstay of investigation is the analysis of congenital reflexes which reflect the maturity if CNS, viability of the newborn and adaptation potential. The following conditions should be fulfilled during examination: comfortable room T (25-26), and it is not recommended to examine the child immediately postprandial or before feeding because feeding determinant can change the level of his congenital reflexes. It should be noted that congenital reflexes of newborns are very labile and are easily fatigued. One should elicit reflexes quickly and turn the child only after cranial and facial skeleton and cranial nerves have been already tested. It is important to look for dysembryological stigmata, which can be frequently encountered: abnormal earlobes (low amount of helixes, absence of earlobes, elongated upper part – rabbit's ear, low set ears), wide nose bridge (hypertelorism), prognatism, low hair border.

25. Special Child: Diagnosis Search premature closure); dolicocephaly (long, narrow head); Slight epicanthalfolds (vertical fold on either side of the nose); Lowset http://www.specialchild.com/diagnosis013.html

Diagnosis Search The parents of this child are anxiously searching for a diagnosis. If you have any information or suggestions you would like to share with them, please send an e-mail to DiagnosisSearch@specialchild.com . Please be sure to mention the name of the child you are referring to so that your message can be immediately forwarded to the parent. Thank you for taking the time to stop by - we appreciate your interest in helping parents with their search. Hayley Kabana, DOB 4/8/94 Features and Characteristics: Hydrocephalus (with VP shunt) Seizures Mild bilateral hearing loss Hypotonia Ligamentous laxity (wears SMOs but can ambulate well) Atrial septal heart defect (repaired) Mental retardation (mild to moderate) Strabismus and sensitive to sunlight Chronic elevated liver enzymes Ketotic hypoglycemia Beau's lines (ridges in the fingernails) Constipation Stridor (a harsh vibratory sound caused by an upper airway obstruction) at night Difficulty maintaining body temperature Mild frontal bossing (prominent forehead) Macrocephaly Flat supraorbital ridges (above the eye cavity) Widely-spaced eyes Downward turned palpebral fissures (opening between the eyelids) Widely-spaced teeth Prominent scaphocephaly (abnormal length and narrowness of the skull as a result of premature closure) Dolicocephaly (long, narrow head)

26. Sotos' Syndrome (www.whonamedit.com) Other principal features are dolicocephaly, macrocrania, hypertelorism, antimongoloidpalpebral slant, higharched palate, frontal bossing, mandibular http://www.whonamedit.com/synd.cfm/2464.html

Home List categories Eponyms A-Z Biographies by country ... Contact Sotos' syndrome Also known as: Nevo's syndrome Sotos' sequence Synonyms: Cerebral gigantism, cerebral gigantism in childhood, constitutional gigantism, gigantismus cerebralis, gigantismus constitutionalis, gigantismus idiopathicus, hypothalamic gigantism, macrostomia-mental retardation syndrome, mental retardation-overgrowth sequence, pituitary gigantism, prenatal gigantism with macrocephaly. Associated persons: S. Nevo Juan Fernandez Sotos Description: A syndrome of excessive growth during the first 4 to 5 years of life, with cerebral gigantism and generalised large muscles in childhood, acromegalic features, and a nonprogressive cerebral disorder with nonprogressive mild mental retardation and defective coordination. After early childhood growth seems to approach normal, remaining, however, two standard deviations above means for chronological age. Birth weight and length greater than normal. Other principal features are dolicocephaly, macrocrania, hypertelorism, antimongoloid palpebral slant, high-arched palate, frontal bossing, mandibular prognathism, and precocious dentition. Occasionally, obesity, convulsions, abnormal dermatoglyphic pattern. Both sexes. Most cases are sporadic but some are transmitted as an autosomal dominant trait. Sotos and collaborators in 1964 first defined this syndrome, which was already well known to paediatricians.

27. Smith-Fineman-Myers Syndrome (Richard D. Smith) (www.whonamedit.com) A rare familial dysmorphysyndrome characterised by microcephaly and dolicocephaly with narrow...... Robert M. Fineman Gart G. Myers Richard D. Smith http://www.whonamedit.com/synd.cfm/2227.html

Home List categories Eponyms A-Z Biographies by country ... Contact Smith-Fineman-Myers syndrome (Richard D. Smith) Synonyms: Short stature-psychomotor retardation-unusual face syndrome. Associated persons: Robert M. Fineman Gart G. Myers Richard D. Smith Description: A rare familial dysmorphy syndrome characterised by microcephaly and dolicocephaly with narrow face,, unusual facies, short stature, chest deformity, mental deficiency, and other dysmorphic features. Eye features include strabismus, short palpebral fissures, hyperopia, and hypoplasia of the optic nerve. Inheritance is X-linked. First described by Smith, Fineman, and Myers on the basis of 2 affected brothers. Bibliography: R. D. Smith, R. M. Fineman, G. G. Myers: Short stature, psychomotor retardation, and unusual facial appearance in two brothers. American Journal of Medical Genetics, New York, 1980, 7: 5-9. L. D. Stephenson, J. P. Johnson: Smith-Fineman-Myers syndrome: report of a third case. American Journal of Medical Genetics, New York, 1985, 22: 301-304 L. C. Ades, B. Kerr, G. Wise:

28. 1Up Health > Health Links Directory > Conditions And Diseases: D Syndrome (5) Digestive Disorders (785) Dimitri Disease (4) Diptheria (6) DissociativeIdentity Disorder (113) Diverticulitis (26) dolicocephaly (3) Down http://www.1uphealth.com/links/conditions-and-diseases-d.html

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 ... Conditions and Diseases : D Description Browse by Alphabets A B C E ... Z Categories Dandy Walker Syndrome De Lange Syndrome Deafblindness Deafness ... Dystonia Musculorum Deformans Help build the largest human-edited directory on the web. Submit a Site Open Directory Project Become an Editor Parts of the directory made available on 1UpHealth have been modified. External Web site links provided on this site are meant for convenience and for informational purposes only; they do not constitute an endorsement. Search: The information provided herein should not be used during any medical emergency or for the diagnosis or treatment of any medical condition. A licensed physician should be consulted for diagnosis and treatment of any and all medical conditions. Call 911 for all medical emergencies. Links to other sites are provided for information only they do not constitute endorsements of those other sites. Home Contact Us Privacy Links Directory

29. Department Of Human Genetics - Clinical Features/Prader-Willi Syndrome _, Characteristic facies with dolicocephaly in infancy, narrow face or bifrontaldiameter, almond shaped eyes , small appearing mouth with thin upper lip http://www.genes.uchicago.edu/ucgs/special-diagnostics/PW-AS/PWfeatures.html

Clinical Features - Prader Willi syndrome It may be helpful to print this page, and keep it with your patients records. Patient's Name: The following is a list of clinical features associated with PWS. This list can also be used as a score sheet for patients suspected to have PWS. Score appropriately, and indicate the total score in the last box. For patients 3 years of age or younger with a score of 5 points, including at least 4 points from the MAJOR Criteria category, the PWS is likely; M-PCR is recommended. M-PCR is also recommended for patients over the age of 3 with a score of 8, with at least 5 points from the MAJOR criteria category. MAJOR Criteria (score 1 point each) Neonatal and infantile central hypotonia with poor suck, gradually improving with age. Feeding problems in infancy with need for special feeding techniques (gavage, premie nipple) and poor weight gain or failure to thrive. Excessive or rapid weight gain on weight for length chart (crossing two percentile channels) after age 12 months but before age 6 years, in the absence of intervention. Characteristic facies with dolicocephaly in infancy, narrow face or bifrontal diameter, "almond shaped eyes", small appearing mouth with thin upper lip, and/or down turned corners of the mouth. (3 or more)

30. AnsMe Directory - Health > Conditions And Diseases > D Dimitri Disease. Diptheria. Dissociative Identity Disorder. Diverticulitis.dolicocephaly. Down Syndrome. Drooling. Dry Eye. Duane Retraction Syndrome. http://dir.ansme.com/health/43346.html

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31. Privattandvård I Örebro, Tandläkaren Michel Deaibes, Sjukdomslista På Engels Dimitri Disease. Diptheria. Dissociative Identity Disorder. Diverticulitis.dolicocephaly. Down Syndrome. Drooling. Dry Eye. Dubowitz Syndrome. Dwarfism. http://www26.brinkster.com/privtand/sjuk.htm

A Aarskog Syndrome Aase Syndrome Abetalipoproteinemia Ablepharon-Macrostomia Syndrome Achilles Tendonitis Achondroplasia Acoustic Neuroma Acromegaly Activated Protein C Resistance Acute Idiopathic Polyneuritis ADD and ADHD Addiction and Recovery Addison's Disease Adiposis Dolorosa Adjustment Disorders Adrenoleukodystrophy Agnosia Agoraphobia Aicardi Syndrome AIDS Alagille Syndrome Albinism Alcoholism Alexander Disease Alkaptonuria Allergies Alopecia Alpers' Disease Alpha1 Antitrypsin Deficiency Alport Syndrome Alstrom Syndrome Alternating Hemiplegia Altophobia Alzheimer's Amblyopia Amputee Amyloidosis Amyoplasia Congenita Amyotrophic Lateral Sclerosis Anal Fissures Anemia Anencephaly Aneurysm Angina Pectoris Anophthalmos Anorexia Anosmia Anterior Knee Pain Syndrome Antiphospholipid Syndrome Anxiety Aortic Valve Disease Apert Syndrome Aphasia Aplastic Anemia Apnea, Sleep Appendicitis Arrhythmia Arteriohepatic Dysplasia Arthritis Arthrogryposis Asbestosis Asperger's Syndrome Aspergillosis Asthma Atherosclerosis Athlete's Foot Atrial Fibrillation Attachment Disorder Attention Deficit Disorder Autism Auto Immune Disorders Aviophobia Aviatophobia B Bacillary Angiomatosis Back Disorders Bad Breath Balanitis Baldness Barth Syndrome Bassen Kornzweig Syndrome Batten Disease Beckwith-Wiedemann Syndrome Behcet's Syndrome Bell's Palsy Benign Breast Lumps Benign Prostatic Hyperplasia Berger's Disease Beriberi Beryllium Disease Besnier Boeck Disease Betalipoprotein Deficiency Disease

32. PPT Slide Facial appearance dolicocephaly Malar hypoplasia Enophthalmos RetrognathiaDownslanting PFs. Skeletal System. Diagnosis Criteria. http://www.mayo.edu/cme-rst/oct2002/01-schowalter/tsld009.htm

PPT Slide Minor findings Moderate pectus excavatum Joint hypermobility High-arched pallate with dental crowding Facial appearance Dolicocephaly Malar hypoplasia Enophthalmos Retrognathia Down-slanting PFs Skeletal System Diagnosis Criteria Previous slide Next slide Back to first slide View graphic version

33. Directory :: Look.com 10) Diarrhoea (25) Digestive Disorders (783) Dimitri Disease (4) Diptheria (4) DissociativeIdentity Disorder (107) Diverticulitis (26) dolicocephaly (3) Down http://www.look.com/searchroute/directorysearch.asp?p=43346

34. Dolicocephaly Similar pages Craniosynostosis For families in Eastern Idaho and parts of Utah. SUBCATEGORIES. Updolicocephaly. America Medica, Inc. ®. info@medlina.com. New York. http://www.medlina.com/dolicocephaly.htm

Academic Medicine Addiction Aging AIDS-HIV ... Women's Health The Web MEDLINA.com (partial) CDC WHO FDA NIH CATEGORIES Search: All Products Books Magazines Popular Music Classical Music Video DVD Baby Electronics Software Outdoor Living Wireless Phones Keywords: Home Up Dolicocephaly Sagittal Synostosis Homepage - http://www.geocities.com Information (including details of genetic research) and support for people affected by this condition. Craniosynostosis - http://www.kidsplastsurg.com Definition, description, diagnosis, treatment and support. Pictures included. Questions and Answers - Craniosyntosis - http://www.neurosurgery.org Frequently asked questions about craniosyntosis, patient and physician resources, and news. SUBCATEGORIES Up powered by A merica M edica, I nc. info@medlina.com New York City

35. Support Groups Sagittal Synostosis Sagittal Synostosis Homepage Sagittal synostosis (also known as scaphocephaly,dolicocephaly, sagittal craniostenosis, or sagittal craniosynostosis), is a http://www.ability.org.uk/support_groups_sagittal_synostos.html

"see the ability, not the disability" You to can help support the Ability Project by: Our Aims ... Z Support Groups Sagittal Synostosis Sagittal Synostosis Homepage - Sagittal synostosis (also known as scaphocephaly, dolicocephaly, sagittal craniostenosis, or sagittal craniosynostosis), is a condition in infants where the sagittal suture (the ‘soft spot’ or fontanelle on top of the head between the left and right sides of the skull) closes early and restricts growth of the head in the side to side direction. This forces the head to grow in a front to back direction, leading to a narrow elongated head. Help build the largest human-edited directory on the web. Submit a Site Open Directory Project Become an Editor Webmaster . Site Design by Ability "see the ability, not the disability" Acknowledgments

36. 3802cr5 bridge and long trunk(4). More recently in 1992, Phelan et al reported a threeyear-oldwith developmental delay, hypotonia, dolicocephaly, ptosis, epicanthal http://www.sma.org.sg/smj/3802/articles/3802cr5.htm

Journals Present Issue Past Issues THESMANEWS Present Issue Past Issues SMJ Editorial Board Letters to the Editor S I N G A P O R E M E D I C A L J O U R N A L This site is supported by Health ONE Partial Monosomy For Chromosome 22 In A Girl With Mental Retardation Y P Yong, L A Knight, M H Yong, S Lam, L Y Ho ABSTRACT This report describes a 5-year 6-month-old Chinese girl with partial monosomy for the long arm of chromosome 22. The karyotype was 46,XX / 46,XX,del (22) (ql3.2). She presented with global developmental delay. Clinical features include seizures, failure-to-thrive, prominent ears, long philtrum and abnormal skin pigmentation on the face and limbs. Keywords: mental retardation, partial monosomy 22 INTRODUCTION Mental retardation in association with physical abnormalities is highly suggestive of chromosomal aberrations. With the availability of increasingly sophisticated techniques in the field of cytogenetics, more patients with so-called idiopathic mental retardation and minor dysmorphic facial features may in reality have an abnormal chromosome karyotype previously undetected. Therefore, mental retardation attributed to chromosomal abnormality will be better defined with increasing awareness and reporting. CASE REPORT Psychological assessment at age 2 years 11 months confirmed global developmental delay with a functional age of approximately 15 months (Bayley’s Scale of Infant development). Subsequent assessment at age 4 years 1 month showed her functioning profile to be about 17 months and speech and language skills at about 12 months.

37. 829: Overlapping Features Of Prader-Willi Syndrome And Trisomy 18 During Infancy She had a narrow bifrontal diameter, dolicocephaly with mild ridging of the sagittaland metopic sutures, almond shaped eyes, a small mouth with a thin upper http://www.faseb.org/genetics/ashg99/f829.htm

Program Nr: 829 Overlapping features of Prader-Willi syndrome and trisomy 18 during infancy. H.A. Ishmael , L.M. Pasztor , P.G. Rothberg , J. Pfotenhauer , V. Hannig , M. Summar , M.G. Butler 1) Section of Medical Genetics and Molecular Medicine, The Children's Mercy Hospitals and Clinics, Kansas City, MO; 2) Division of Medical Genetics, Department of Pediatrics, Vanderbilt University, Nashville, TN.

38. Untitled dysmorphic features include dysplastic toenails, relatively large fleshy hands,prominent and/or dysplastic ears, pointed chin, dolicocephaly, ptosis, and http://www.faseb.org/genetics/ashg01/f95.htm

Program Nr: 95 Deletion 22q13 syndrome - under-recognized and under-diagnosed. M.C. Phelan , R.C. Rogers , D.B. Everman , G.A. Stapleton , N.R. Powers , S.R. Shaw 1) T C Thompson Children's Hosp, Chattanooga, TN; 2) Greenwood Genetic Center, Greenwood, SC; 3) The Children's Hospital, Greenville, SC.

39. A Guide To Pathology - Medical Books By Dr K Chaudhry, New Delhi includes (i) A tendency to great height (ii) Long and thin hands and feet (iii)Spinal curvatures ; Qv) Funnel or pigeon chest (v) dolicocephaly and bossing http://medicalbooks.rushsale.net/pathology/chapter14.php

40. Sci.anthropology.paleo: Re: Homo Heidelbergensis ridges (I can feel mine distinctly), second toes longer than first toes (well,mine are), relative dolicocephaly (at ^^^^^ least http://www.anatomy.usyd.edu.au/danny/anthropology/sci.anthropology.paleo/archive

Re: Homo heidelbergensis Xiaoguang Zhang ( zhang@gmsds.ms.ornl.gov Sun, 5 Jun 1994 21:01:30 GMT Messages sorted by: [ date ] [ thread ] [ subject ] [ author ] Next message: Cameron Laird: "Re: aquatic ape?" Previous message: Stanley Friesen: "Re: Early diets" Maybe in reply to: NICHOLLS PHILIP A: "Homo heidelbergensis" Ken Brown (rkjb@cix.compulink.co.uk) wrote: : Back on topic for a while - I have a purely sentimental attraction to the : idea that some of the oddities about us northern Europeans are due to : Partial albinism, vestigal brow ridges (I can feel mine distinctly), second : toes longer than first toes (well, mine are), relative dolicocephaly (at : least amongst early populations, it seems to have diminished in the last : millenium)... until someone proves the contrary with genetic evidence I shall : persist in imagining that I have a few Neanderthal ancestors! I wonder if this constitutes counter argument: I'm a Chinese, and my second toes are longer than first toes. Same for my wife (also a Chinese). Does that mean that I too have a few Neanderthal ancestors?

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