نتایج جستجو برای: angelman syndrome
تعداد نتایج: 621986 فیلتر نتایج به سال:
Facts about AS was initially a small booklet developed in 1987 to help launch the Angelman Syndrome Foundation organization and to help inform parents and professionals about the syndrome. The Facts document is now in its seventh edition. Over the years, it has grown in scope and complexity and this year the " pamphlet/brochure" has been reformatted for a web presence. Current authors are:
Autism is a common neurodevelopmental disorder of complex genetic etiology. Rett syndrome, an X-linked dominant disorder caused by MECP2 mutations, and Angelman syndrome, an imprinted disorder caused by maternal 15q11-q13 or UBE3A deficiency, have phenotypic and genetic overlap with autism. MECP2 encodes methyl-CpG-binding protein 2 that acts as a transcriptional repressor for methylated gene c...
Angelman syndrome is one of the most studied human diseases related to a gene that is expressed on the maternal chromosome only in at least some brain cells. It is caused by inactivation of the UBE3A gene in the brain due to various abnormalities of the 15q11-q13 chromosome inherited from the mother. It is characterized by severe developmental delay, seizures, virtual absence of speech, motor i...
Rett and Angelman syndromes comprise part of the spectrum of neurologic disorders associated with autism. Their clinical presentations overlap, with both presenting in later infancy with global developmental delays, severe speech and communication impairments, progressive microcephaly, seizures, autistic behaviors, and characteristic albeit different movement disorders and stereotypic hand move...
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