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1 синдром Ротмунда
1) Medicine: Rothmund's syndrome (дистрофия; наследственно обусловленное сочетание атрофической пойкилодермии и катаракты)2) Pediatrics: Rothmund syndrome -
2 дистрофия Ротмунда
Medicine: Rothmund's syndrome (наследственно обусловленное сочетание атрофической пойкилодермии и катаракты)Универсальный русско-английский словарь > дистрофия Ротмунда
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3 наследственная пойкилодерма
ж.congenital poikiloderma, Rothmund's syndromeБольшой русско-английский медицинский словарь > наследственная пойкилодерма
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4 синдром Ротмунда
педиатр. Rothmund(-Thomson) syndromeБольшой русско-английский медицинский словарь > синдром Ротмунда
См. также в других словарях:
Rothmund-Thomson syndrome — Infobox Disease Name = PAGENAME Caption = DiseasesDB = 29891 ICD10 = ICD9 = ICD9|757.33 ICDO = OMIM = 268400 MedlinePlus = eMedicineSubj = derm eMedicineTopic = 379 MeshID = D011038Rothmund Thomson Syndrome is a rare autosomal recessive [cite… … Wikipedia
Rothmund-Thomson syndrome (RTS) — An hereditary disease characterized by progressive degeneration (atrophy), scarring and abnormal pigmentation of the skin together with stunting of growth, baldness, cataracts, depressed nasal bridge, and malformations of the teeth, nails and… … Medical dictionary
Rothmund-Thomson syndrome — Roth·mund Thom·son syndrome (rotґmoond tomґson) [August von Rothmund, Jr., German physician, 1830–1906; Mathew Sidney Thomson, English dermatologist, 1894–1969] see under syndrome … Medical dictionary
Rothmund-Thomson syndrome — an autosomal recessive syndrome characterized by reticulated, atrophic, hyperpigmented, telangiectatic cutaneous plaques, often with juvenile cataracts, saddle nose, congenital bone defects, disturbances in growth of hair, nails, and teeth, and… … Medical dictionary
RTS (Rothmund-Thomson syndrome) — An hereditary disease characterized by progressive degeneration (atrophy), scarring and abnormal pigmentation of the skin together with stunting of growth, baldness, cataracts, depressed nasal bridge, and malformations of the teeth, nails and… … Medical dictionary
Syndrome de rothmund-thomson — Autre nom Poïkilodermie de Rothmund Thomson Référence MIM … Wikipédia en Français
Syndrome de Rothmund-Thomson — Référence MIM 268400 Transmission Récessive Chromosome 8q24.3 Gène RECQL4 Empreinte parentale Non … Wikipédia en Français
Rothmund-Thomson-Syndrom — Klassifikation nach ICD 10 Q82.8 Sonstige näher bezeichnete angeborene Fehlbildungen der Haut … Deutsch Wikipedia
Syndrome, Rothmund-Thomson — An hereditary disease characterized by progressive degeneration (atrophy), scarring and abnormal pigmentation of the skin together with stunting of growth, baldness, cataracts, depressed nasal bridge, and malformations of the teeth, nails and… … Medical dictionary
Syndrome de baller-gerold — Pour les articles homonymes, voir Gérold. Syndrome de Baller Gerold … Wikipédia en Français
Syndrome Rapadilano — Référence MIM 266280 Transmission Récessive Chromosome 8q24.3 Gène RECQL4 Mutation Ponctuelle … Wikipédia en Français
