Alpha-thalassemia/mental retardation syndrome X-linked (ATRX; OMIM #301040), which is caused by mutations in the gene, is characterized by alpha-thalassemia, distinct dysmorphic facies, psychomotor development delay and genital abnormalities. Here, we describe a neonatal case of syndromic disorder of sex development, harboring a novel hemizygous mutation, p.Asp2352fs*1 in the carboxyl-terminal domain of . Our study provides additional evidence that deletion of the carboxyl terminus of ATRX is associated with severe genital anomalies.
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| http://dx.doi.org/10.1038/hgv.2017.12 | DOI Listing |
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