Mohr syndrome

Mohr syndrome
an autosomal recessive disorder characterized by brachydactyly, clinodactyly, polydactyly, syndactyly, and bilateral hallucal polysyndactyly; by cranial, facial, lingual, palatal, and mandibular anomalies; and by episodic neuromuscular disturbances. Called also orodigitofacial dysostosis, oral-facial-digital s., type II, and orofaciodigital s., type II. See also oral-facial-digital s., type I.

Medical dictionary. 2011.

Нужно решить контрольную?

Look at other dictionaries:

  • Mohr syndrome — (mor) [Otto Lous Mohr, Norwegian geneticist, 1886–1967] see under syndrome …   Medical dictionary

  • Mohr–Tranebjærg syndrome — Classification and external resources OMIM 304700 Mohr–Tranebjærg syndrome (MTS) is a rare X liked recessive syndrome also known as Deafness dystonia syndrome and caused by mutation in the TIMM8A gene. It was first described in 1960 …   Wikipedia

  • Syndrome de mohr-tranebjaerg — Autre nom Syndrome surdité dystonie neuropathie optique Référence MIM …   Wikipédia en Français

  • Syndrome de Mohr-Tranebjaerg — Référence MIM 304700 Transmission Récessive liée à l X Chromosome Xq22 Gène TIMM8A Empreinte parentale Non …   Wikipédia en Français

  • Syndrome dépressif — Dépression (psychiatrie) Pour les articles homonymes, voir Dépression. Las de la vie Peinture de Ferdinand Hodler (18 …   Wikipédia en Français

  • 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

  • Jan Mohr — Jan Gunnar Faye Mohr, Norwegian Danish physician and geneticist. Known for his discovery of the first cases of autosomal genetic linkage in man, between the Lutheran blood groups and the ABH secretor system, and between these and the hereditary… …   Wikipedia

  • Orofaciodigital syndrome 1 — Classification and external resources OMIM 311200 DiseasesDB 29898 MeSH …   Wikipedia

  • Orofaciodigital syndrome — type I (OFD1) is an X linked disorder characterized by malformations of the face, oral cavity, and digits with polycystic kidney disease and variable involvement of the central nervous system. cite journal author=Badano JL, Mitsuma N, Beales PL,… …   Wikipedia

  • oral-facial-digital syndrome type II — Mohr s …   Medical dictionary

Share the article and excerpts

Direct link
Do a right-click on the link above
and select “Copy Link”