| Literature DB >> 30179896 |
Roger E Stevenson1, Albert E Chudley2, Anand K Srivastava1, Jayson Rodriguez1, Michael J Friez1, Charles E Schwartz1.
Abstract
UBE2A-related X-linked intellectual disability is characterized by a distinctive facial phenotype (dense eyebrows and eyelashes, synophrys, hypertelorism, upslanted palpebral fissures, wide mouth, and thin lips), generalized hirsutism, hypoplastic genitalia, short stature, hypotonia, seizures, and severe intellectual disability. Five affected males in two families are described here and compared with the previously reported 17 males in eight families. The new cases are notable for the absence of nail dystrophy, previously considered a defining manifestation, and for the presence of hypogammaglobulinemia and adult-onset ataxia.Entities:
Mesh:
Substances:
Year: 2019 PMID: 30179896 PMCID: PMC6279472 DOI: 10.1097/MCD.0000000000000242
Source DB: PubMed Journal: Clin Dysmorphol ISSN: 0962-8827 Impact factor: 0.816