acrocephalopolysyndactyly type IV

acrocephalopolysyndactyly type IV
Goodman syndrome.

Medical dictionary. 2011.

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  • acrocephalopolysyndactyly type I — Pfeiffer syndrome …   Medical dictionary

  • acrocephalopolysyndactyly type II — Carpenter syndrome …   Medical dictionary

  • acrocephalopolysyndactyly type III — Sakati Nyhan syndrome …   Medical dictionary

  • acrocephalopolysyndactyly — A group of congenital syndromes characterized by abnormal skull shape due to craniosynostosis, brachydactyly, syndactyly, and preaxial polydactyly of hands and/or feet; mental retardation is a …   Medical dictionary

  • Acrocephalosyndactylia — Infobox Disease Name = PAGENAME Caption = DiseasesDB = ICD10 = ICD10|Q|87|0|q|80 ICD9 = ICD9|755.55 ICDO = OMIM = MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = D000168 Acrocephalosyndactylia (or acrocephalosyndactyly) is the common… …   Wikipedia

  • Sakati-Nyhan-Tisdale syndrome — Sakati Nyhan Tisdale Syndrome,cite web | title = Sakati Nyhan Tisdale Syndrome Information | publisher = Ole Daniel Enersen | url = http://www.whonamedit.com/synd.cfm/2176.html] also called acrocephalopolysyndactyly type III, is a rare genetic… …   Wikipedia

  • Pfeiffer syndrome — A form of craniosynostosis that results in multiple physical defects, including broad thumbs and great toes; depressed nasal bridge and generally flat profile; low set, slanted ears;, strabismus; and a prominent mandible. There may also be… …   Medical dictionary

  • Carpenter syndrome — Infobox Disease Name = PAGENAME Caption = DiseasesDB = 29583 ICD10 = ICD9 = ICDO = OMIM = 201000 MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = Carpenter syndrome, also called acrocephalopolysyndactyly type II, [OMIM|201000] is an… …   Wikipedia

  • Carpenter syndrome — an autosomal recessive disorder characterized by acrocephaly with polysyndactyly, brachydactyly, mental retardation, mild obesity, hypogonadism, and other anomalies. It is believed to encompass disorders formerly distinguished as Goodman syndrome …   Medical dictionary

  • Sakati-Nyhan syndrome — an autosomal dominant disorder characterized by acrocephaly and polysyndactyly with hypoplastic tibias and deformed, displaced fibulas. Called also acrocephalopolysyndactyly, type III …   Medical dictionary

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