marfanoid

marfanoid
Apparently similar to Marfan syndrome, but not necessarily associated with the elastin gene.

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  • Marfanoid — (or Marfanoid habitus) is a term used to describe a constellation of findings including long limbs, arachnodactyly and hyperlaxity. Associated conditions include: Marfan syndrome (the source of the name) Multiple endocrine neoplasia type 2B[1][2] …   Wikipedia

  • marfanoid — A term used of those whose phenotype bears a superficial resemblence to that of Marfan syndrome. * * * mar·fa·noid mär fə .nȯid adj exhibiting the typical characteristics of Marfan syndrome <the marfanoid habitus> * * * mar·fan·oid… …   Medical dictionary

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  • Multiple endocrine neoplasia type 2 — MEN type 2A (Sipple syndrome) Classification and external resources Bilateral pheochromocytomas associated with Multiple endocrine neoplasia type 2 ICD 10 D …   Wikipedia

  • DHHC domain — A depiction of the topology of DHHC family palmitoyltransferases. Transmembrane alpha helices are represented as black tubes. The DHHC domain is shown as a light orange oval. Identifiers Symbol DHHC …   Wikipedia

  • Multiple endocrine neoplasia — Classification and external resources Micrograph of a medullary thyroid carcinoma, as may be seen in MEN 2A and MEN 2B. H E stain …   Wikipedia

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  • Malouf syndrome — (also known as congestive cardiomyopathy hypergonadotropic hypogonadism syndrome ) is a congenital disorder that causes one or more of the following symptoms: mental retardation, ovarian dysgenesis, congestive cardiomyopathy, broad nasal base,… …   Wikipedia

  • Hypermobility — Classification and external resources [[File: |frameless|upright=1.06|alt=]] Hypermobile fingers and thumb ICD 10 M35.7 …   Wikipedia

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