- Wolf-Hirschhorn syndrome
- Wolf-Hirschhorn syndrome.(Источник: «Англо-русский толковый словарь генетических терминов». Арефьев В.А., Лисовенко Л.А., Москва: Изд-во ВНИРО, 1995 г.)
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Wolf-Hirschhorn syndrome
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Wolf–Hirschhorn syndrome — Wolf Hirschhorn syndrome Classification and external resources ICD 10 Q93.3 ICD 9 758.3 … Wikipedia
Wolf-Hirschhorn syndrome — Infobox Disease Name = Wolf Hirschhorn syndrome Caption = DiseasesDB = 32279 ICD10 = ICD10|Q|93|3|q|90 ICD9 = ICD9|758.3 ICDO = OMIM = 194190 MedlinePlus = eMedicineSubj = ped eMedicineTopic = 2446 MeshID = Wolf Hirschhorn syndrome, also known as … Wikipedia
Wolf-Hirschhorn syndrome (WHS) — is a chromosome disorder due to partial deletion of the short (p) arm of chromosome 4. It is therefore also called the 4p syndrome. Features of the syndrome include midline defects with a scalp defect, widespaced eyes, broad or beaked nose, oral… … Medical dictionary
Wolf-Hirschhorn syndrome — Wolf Hirsch·horn syndrome (voolfґ hurshґhorn) [Ulrich Wolf, German physician, born 1933; Kurt Hirschhorn, American physician, born 1926] see under syndrome … Medical dictionary
Wolf-Hirschhorn syndrome — a syndrome associated with partial deletion of the short arm of chromosome 4, characterized by microcephaly, ocular hypertelorism, epicanthus, cleft palate, micrognathia, low set ears simplified in form, cryptorchidism, and hypospadias … Medical dictionary
Syndrome de wolf-hirschhorn — Le syndrome de Wolf Hirschhorn est une maladie chromosomique associant : faciès caractéristique, retard de croissance intra utérin suivi d’un retard de croissance post natal, hypotonie musculaire, retard de développement avec un retard… … Wikipédia en Français
Syndrome, Wolf-Hirschhorn — Wolf Hirschhorn syndrome (WHS) is a chromosome disorder due to partial deletion of the short (p) arm of chromosome 4. It is, therefore, also called the 4p syndrome. Features of the syndrome include midline defects with a scalp defect, widespaced… … Medical dictionary
Wolf-Hirschhorn Syndrom — Das Wolf Hirschhorn Syndrom (auch als Wolf Syndrom oder Chromosom 4p Syndrom bekannt) ist eine seltene angeborene Erbkrankheit, die durch eine sogenannte strukturelle Chromosomenaberration am kurzen Arm des Chromosom 4 bedingt ist. Leitsymptom… … Deutsch Wikipedia
Wolf-Hirschhorn-Syndrom — Klassifikation nach ICD 10 Q93.3 Deletion des kurzen Armes des Chromosoms 4 Wolf Hirschhorn Syndrom … Deutsch Wikipedia
Syndrome de Wolf-Hirschhorn — Le syndrome de Wolf Hirschhorn est une maladie chromosomique associant : faciès caractéristique, retard de croissance intra utérin suivi d’un retard de croissance post natal, hypotonie musculaire, retard de développement avec un retard… … Wikipédia en Français
