نتایج جستجو برای: autosomal recessive primary microcephaly

تعداد نتایج: 682552  

Journal: :Journal of medical genetics 2011
Nuria Rivera-Brugués Beate Albrecht Dagmar Wieczorek Heinrich Schmidt Thomas Keller Ina Göhring Arif B Ekici Andreas Tzschach Masoud Garshasbi Kathlen Franke Norman Klopp H-Erich Wichmann Thomas Meitinger Tim M Strom Maja Hempel

BACKGROUND Cohen syndrome is a rare autosomal recessive disorder with a complex phenotype including psychomotor retardation, microcephaly, obesity with slender extremities, joint laxity, progressive chorioretinal dystrophy/myopia, intermittent isolated neutropenia, a cheerful disposition, and characteristic facial features. The COH1 gene, which contains 62 exons, is so far the only gene known t...

Journal: :Oncology reports 2008
Carsten Hagemann Jelena Anacker Stefanie Gerngras Siglinde Kühnel Harun M Said Rajnikant Patel Ulrike Kämmerer Dirk Vordermark Klaus Roosen Giles Hamilton Vince

Patients with autosomal recessive primary microcephaly have a small but architecturally normal brain containing a reduced number of neurons. Microcephalin and ASPM are two of the genes causing this disease. Both are centrosomal proteins involved in cell cycle regulation. Whereas microcephalin is a component of the DNA damage response and a repressor of telomerase function, ASPM is required for ...

Journal: :Journal of Investigative Dermatology 2009

Journal: :Orphanet Journal of Rare Diseases 2006

Journal: :American journal of medical genetics. Part A 2006
Anna Rajab Seung-Yun Yoo Aiman Abdulgalil Salem Kathiri Riaz Ahmed Ganeshwaran H Mochida Adria Bodell A James Barkovich Christopher A Walsh

Cerebral palsy (CP) is defined as any nonprogressive motor deficits resulting from cerebral abnormalities that occur in the prenatal or perinatal period. Symptoms become apparent during the first year of life. Genetic forms of CP account for about 2% in European populations but are thought to cause a substantial proportion in consanguineous families. We have identified a large consanguineous fa...

Journal: :Journal of Clinical Pathology 1988

Journal: :American Journal of Medical Genetics 1989

Backgrounds: Hypohidrotic ectodermal dysplasia (HED) is a rare genetic disorder, distinguished by hypotrichosis, hypohidrosis, and hypodontia. HDE can be inherited in X-linked recessive manner as a result of mutations in the ectodysplasin A (EDA) gene as well as autosomal dominant and autosomal recessive manners both of them caused by mutations in EDA receptor (EDAR) and EDAR-associated death d...

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