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Rothmund syndrome

См. также в других словарях:

  • 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

  • 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

  • Rothmund-Thomson-Syndrom — Klassifikation nach ICD 10 Q82.8 Sonstige näher bezeichnete angeborene Fehlbildungen der Haut …   Deutsch Wikipedia

  • 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

  • syndrome — The aggregate of symptoms and signs associated with any morbid process, and constituting together the picture of the disease. SEE ALSO: disease. [G. s., a running together, tumultuous concourse; (in med.) a concurrence of symptoms, fr. syn,… …   Medical dictionary

  • Syndrome de Baller-Gerold — Pour les articles homonymes, voir Gérold. Syndrome de Baller Gerold Référence MIM 218600 Transmission Récessive Chromosome …   Wikipédia en Français

  • 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 (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

  • 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

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