| Literature DB >> 27297501 |
Wuyan Chen1, Ashley F Perritt2, Rachel Morissette2, Jennifer L Dreiling3, Markus-Frederik Bohn4, Ashwini Mallappa2, Zhi Xu5, Martha Quezado3, Deborah P Merke2,6.
Abstract
Some variants that cause autosomal-recessive congenital adrenal hyperplasia (CAH) also cause hypermobility type Ehlers-Danlos syndrome (EDS) due to the monoallelic presence of a chimera disrupting two flanking genes: CYP21A2, encoding 21-hydroxylase, necessary for cortisol and aldosterone biosynthesis, and TNXB, encoding tenascin-X, an extracellular matrix protein. Two types of CAH tenascin-X (CAH-X) chimeras have been described with a total deletion of CYP21A2 and characteristic TNXB variants. CAH-X CH-1 has a TNXB exon 35 120-bp deletion resulting in haploinsufficiency, and CAH-X CH-2 has a TNXB exon 40 c.12174C>G (p.Cys4058Trp) variant resulting in a dominant-negative effect. We present here three patients with biallelic CAH-X and identify a novel dominant-negative chimera termed CAH-X CH-3. Compared with monoallelic CAH-X, biallelic CAH-X results in a more severe phenotype with skin features characteristic of classical EDS. We present evidence for disrupted tenascin-X function and computational data linking the type of TNXB variant to disease severity.Entities:
Keywords: CAH-X; Ehlers-Danlos syndrome; biallelic; congenital adrenal hyperplasia; tenascin-X
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Year: 2016 PMID: 27297501 PMCID: PMC4983206 DOI: 10.1002/humu.23028
Source DB: PubMed Journal: Hum Mutat ISSN: 1059-7794 Impact factor: 4.878