81. Micropenis Indications, causes, and treatment.Category Health Men s Health Conditions and Diseases Microphallus...... micropenis. robinow syndrome mesomelic dwarfism, dental anomalies.LH receptor defect/mutation. 5a -reductase type 2 deficiency, Usually http://www.kids-urology.com/micropenis.html

Micropenis Description: Epidemiology Statistical definition based on stretched penile length Incidence – Statistically, occurs in 0.6% of population Normal newborn penis is at least 1.9 cm long The term micropenis should not be used with other abnormalities of the penis, e.g., hypospadias Environmental factors - none Genetics – there is no genetic determinant for micropenis, but some genetic syndromes are associated with it Chromosomes – abnormal number, e.g., Klinefelter and Down syndromes Genes – genetic mutation, e.g., androgen insensitivity ("Testicular Feminization") Signs and Symptoms Signs - Small penis Symptoms - n one unless part of a syndrome Pathology/Pathophysiology Penile development includes androgen dependent and independent growth Majority of development depends on secretion of androgens First 3 months of gestation Maternal HCG causes fetal testis Leydig cells to produce testosterone Testosterone converted to dihydrotestosterone in genital tubercle by 5a-reductase type 2 Penis and urethra become completely formed during first trimester Fourth month of gestation onward Fetal hypothalamus and pituitary drive testosterone production by testi s Micropenis is generally due to inadequate testosterone stimulation during 2 nd and 3 rd trimester of gestation Additional growth at puberty, ages 11-18, due to increase in serum testosterone to adult levels

82. R Index RING CHROMOSOME 6. RING CHROMOSOME 9. RISK. robinow syndrome. RUBELLA, CONGENITAL.RUBINSTEINTAYBI SYNDROME. RUNAWAY CHILDREN. RUSSELL-SILVER SYNDROME. http://www.childhealthinfo.com/rindex.htm

ChildHealthInformation Center - The Online Database A B C D ... Z Please click on the "box below" to view the following topics. R Part I RABIES (HYDROPHOBIA) RACISM RADIATION RADIOLOGY RADON RAPE RARE DISORDERS RASMUSSEN SYNDROME READING RECKLINGHAUSEN DISEASE RECOVERY REFLEX SYMPATHETIC DYSTROPHY SYNDROME REFSUM DISEASE REHABILITATION Please click on the "box below" to view the following topics. R Part II RENDU-OSLER-WEBER SYNDROME REPETITIVE MOTION SYNDROME REPRODUCTIVE MEDICINE RESPIRATORY DISEASES RESPIRATORY PAPILLOMATOSIS, RECURRENT RESTLESS LEGS SYNDROME RETINITIS PIGMENTOSA RETINOBLASTOMA RETINOPATHY OF PREMATURITY (ROP) RETT SYNDROME REYE'S SYNDROME RHEUMATOID ARTHRITIS RIGHT TO DIE RILEY-DAY SYNDROME RING CHROMOSOME 15 RING CHROMOSOME 18 RING CHROMOSOME 21 RING CHROMOSOME 22 RING CHROMOSOME 4 RING CHROMOSOME 6 RING CHROMOSOME 9 RISK ROBINOW SYNDROME RUBELLA, CONGENITAL RUBINSTEIN-TAYBI SYNDROME RUNAWAY CHILDREN RUSSELL-SILVER SYNDROME [Home] [Printed Guide] [Child Care for the '90's] MoreInfo@ChildHealthInfo.com

83. Robinow's Syndrome (www.whonamedit.com) robinow's syndrome A syndrome of multiple cogenital anomalies, including foetallikefacies, mesomelic dwarfism, and genital hypoplasia. robinow's syndrome http://www.whonamedit.com/synd.cfm/3020.html

Home List categories Eponyms A-Z Biographies by country ... Contact Robinow's syndrome Also known as: Robinow's dwarfism Robinow-Silverman-Smith syndrome Synonyms: Achondroplasialike dwarfism syndrome, achondroplastic dwarfism syndrome, acral dysostosis with facial and genital abnormalities, foetal face-mesomelic dwarfism, foetal-face syndrome, mesomelic dwarfism-small genitalia syndrome, mesomelic dwarfism syndrome. Associated persons: Meinhard Robinow Frederic N. Silverman Hugo D. Smith Description: A rare syndrome characterized by unusual (foetal-like) facies, mesomelic shortening of the forearms, hemivertebrae, genital hypoplasia, frontal bossing, hypertelorism, wide palpebral fissures, short upturned nose with anteverted nares, long philtrum, receding chin, brachydactyly, and a long list of other anomalies. Both sexes affected. Present from birth. Intelligence is usually normal but delayed physical and mental development noted in about 18%. Inheritance is usually autosomal dominant but recessive and sporadic cases have been reported. First described by Robinow et al on the basis of a family with affected persons in six generations. Bibliography: M. Robinow, F. N. Silverman, H. D. Smith:

84. Meinhard Robinow (www.whonamedit.com) geneticist, born May 19, 1909, Hamburg, died July 1997. Associatedwith robinow's syndrome,robinowSorauf syndrome. Who named it? http://www.whonamedit.com/doctor.cfm/2554.html

Home List categories Eponyms A-Z Biographies by country ... Contact Meinhard Robinow German-American paediatrician and clinical geneticist, born May 19, 1909, Hamburg, died July 1997. Associated eponyms: Robinow's syndrome A syndrome of multiple cogenital anomalies, including foetal-like facies, mesomelic dwarfism, and genital hypoplasia. Robinow-Sorauf syndrome A syndrome of facies like those of the Sæthre-Chotzen syndrome and bilaterally broad big toes owing to partial or complete duplication of the distal phalanx. Biography: Meinhard Robinow was the son of a Hamburg lawyer. He studied medicine at the Universities of Munich, Heidelberg, Berlin and Hamburg, graduating in 1934. Shortly after he moved to the USA to avoid Nazi persecution. He subsequently trained in paediatrics in Augusta, Georgia and at the Fels Research Institute, Yellow Springs, Ohio. After serving in the US Army Medical Corps in Europe during World War II, he settled in paediatric practice in Yellow Springs, Ohio. He remained here until 1975, when he accepted an academic position at the University of Virginia. From here he moved to Wright State University and the Children's Medical Center in Dayton, Ohio. Robinow spent the last years of his life on a farm in Ohio with his wife since 1944, Beatrice Wilt. They had three children. Ole Daniel Enersen

85. Les Liens Syndrome De Robinow Translate this page Rare Genetic Diseases In Children Gateway Kiosk Support Group Forum robinowsyndrome. (adresse Fondation sur le syndrome de robinow. Association http://www.ifrance.com/nikomanue/Liens.html

Quelques liens THE ROBINOW (FETAL FACE) SYNDROME ( adresse : http://baserv.uci.kun.nl/~mvanstee/robinow.html ) Son email est : m.vansteensel@antrg.azn.nl Rare Genetic Diseases In Children: Gateway Kiosk Support Group Forum : Robinow Syndrome (adresse : http://mcrcr2.med.nyu.edu/murphp01/robsupt.htm) Le "Gateway Kiosk" est un site qui référence les ressources disponibles sur différents syndromes, dont le syndrome de Robinow. Vous y trouverez une présentation de M Vansteensel ainsi que de la page présentée précédemment, une présentation de la Fondation sur le Syndrome de Robinow (voir plus bas), ainsi qu'un "forum" avec des messages et questions de personnes ou familles concernées par le syndrome. Fondation sur le syndrome de Robinow http://www.robinow.org Robinow Syndrome Foundation P.O. Box 1072 Anoka, MN 55303 Ph: 612.434.1152 Fax: 612.434.3691 ou bien : Robinow Syndrome Foundation 15955 UPLANDER STREET NW ANDOVER, MINNESOTA 55304-2501 EMAIL : ortizk7506@aol.com

86. Robinow's Syndrome one click For Medical Professionals only. robinow's syndrome,,Print this article, (Meinhard robinow, born 1909, American physician http://www.amershamhealth.com/medcyclopaedia/Volume VII/ROBINOWS SYNDROME.asp

Medcyclopaedia About Medcyclopaedia Amersham Health Search for: Type a word or a phrase. All forms of the word are searchable. Advanced search Browse entry words starting with: A B C D ... Other characters Try our Medcyclopaedia Premium Edition with added tools and functionality tailored to make your working day easier. The following tools are presently available: Expanded search *For Medical Professionals only, registration required Robinow's syndrome, (Meinhard Robinow, born 1909, American physician), see mesomelic dysplasia HC The Encyclopaedia of Medical Imaging Volume VII Welcome to Medcyclopaedia. This site is open to a public audience, still we want to know a little more about our visitors. Please tick off the boxes that match your profile. Do you live in Europe? Yes No Are you a medical professional? Yes No This frame will disappear when submitted Legal Contact us Making Waves

87. UNSW Embryology-OMIM PIERRE ROBIN SYNDROME AND OLIGODACTYLY expressed the opinion that this disorder is the same as that named 'postaxial acrofacialdysostosis syndrome' (263750) by Miller et al. (1979). robinow et al. http://anatomy.med.unsw.edu.au/cbl/embryo/OMIMfind/head/OMIM-172880.htm

UNSW Embryology HEAD AND NECK DEVELOPMENT Embryology Home Page PIERRE ROBIN SYNDROME AND OLIGODACTYLY Select Entry from OMIM Online Mendelian Inheritance in Man (Internet Link) This page is for computers without external internet access. Back to UNSW Embryology-Head and Neck Notes List of OMIM search results Pierre Robin Syndrome 172880 PIERRE ROBIN SYNDROME AND OLIGODACTYLY Alternative titles; symbols ROBIN SEQUENCE AND OLIGODACTYLY TABLE OF CONTENTS TEXT REFERENCES CREATION DATE EDIT HISTORY ... CLINICAL SYNOPSIS Database Links Note: pressing the symbol will find the citations in MEDLINE whose text most closely matches the text of the preceding OMIM paragraph, using the Entrez MEDLINE neighboring function. TEXT Robinow et al. (1986)

88. Robinowin Oireyhtymä sukuelinten poikkeavuudet. robinowin oireyhtymä. robinowin dvarfismi robinowSilverman-Smithinoireyhtymä Fetaalisten kasvojen oireyhtymä. http://www.saunalahti.fi/kup/syndroma/robinow.htm

Kehitysvammahuollon tietopankki Raajojen luutumishäiriö ja kasvojen sekä sukuelinten poikkeavuudet Robinowin oireyhtymä Robinowin dvarfismi Robinow-Silverman-Smithin oireyhtymä Fetaalisten kasvojen oireyhtymä Oireyhtymän pääpiirteet ovat fetaaliset kasvot (sikiöaikaisen näköiset), vajaamittaiset kyynervarret, kohoava otsa, etäiset silmät ( hypertelorismi ), leveät ja alaspäin vinot silmäluomiraot, ylöspäin kääntynyt leveä nenä ja sieraimet, pitkä ylähuulivako, taakse vetäytynyt leuka, lyhytsormisuus ja vajaakasvuiset sukuelimet. Älyllinen suoriutuminen on yleensä normaalia, mutta psyykkistä kehitysvammaisuutta ja kasvuviivettä esiintyy noin 18 %:lla. Pää on yleensä suuri ( makrokefalia ), korvalehdet poikkeavan näköiset ja ylähuuli V:n muotoinen tai telttamainen. Huuli- ja kitalaenhalkio, suulaen lyhyys, hampaiden virheasentoisuus, ikenien vetäytyminen, kitakielekkeen epämuodostuminen ja kielen jäykkyys saattavat niinikään kuulua oireisiin, samoin kylkiluiden epämuodostumat, kuopparintaisuus ja nivuksen tai napanuoran tyrä. Pienikokoisten käsien viidennet sormet ovat usein vinot. Sekä sormet että varpaat ovat lyhyet. Myös jalat ovat pienikokoiset.

89. Health Library Ringworm of the Skin. Risedronate for osteoporosis. Roberts syndrome. Robinowsyndrome. Rocky Mountain Spotted Fever. Romano Ward syndrome. Root canal. http://health_info.nmh.org/Library/HealthGuide/IllnessConditions/_SearchResults.

90. Katalog - Wirtualna Polska Serwis Katalog w Wirtualna Polska S.A. pierwszy portal w Polsce. http://katalog.wp.pl/DMOZ/Health/Conditions_and_Diseases/Genetic_Disorders/Robin

Poczta Czat SMS Pomoc Szukaj.wp.pl: -Katalog -Polskie www -¦wiatowe www -Wirtualna Polska -FTP/Pliki -Grupy dyskusyjne -Encyklopedia -Produkty wp.pl Katalog Katalog ¦wiatowy DMOZ ... Conditions and Diseases > Genetic Disorders Fakty o Katalogu Pomoc Regulamin Serwis szukaj ... Ostatnio dodane NAWIGACJA Fakty o katalogu Pomoc Regulamin Serwis Szukaj ... FAQ Dodaj stronê Katalog WP Polskie Strony WWW Oferta dla firm WP-HIT ... Wirtualna Polska

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