Institute of Medical Genetics, Charité Universitätsmedizin, Berlin, Germany.
Am J Med Genet A. 2010 Apr;152A(4):870-4. doi: 10.1002/ajmg.a.33301.
Craniometaphyseal dysplasia (CMD) is a rare, sclerosing skeletal disorder caused by mutations in ANKH, which encodes a putative pyrophosphate transporting membrane protein. Six distinct ANKH mutations have been described to date. We report here on three novel mutations in simplex patients with CMD. The c.1015T>C (p.Cys339Arg) mutation found in Patient A was associated with congenital facial palsy, early-onset conductive hearing loss, and a generalized undermodeling of the long bones. The c.1172T>C (p.Leu391Pro) mutation in Patient B was associated with facial palsy, progressive conductive hearing loss, and generalized undermodeling of tubular bones. A milder phenotype without cranial nerve affection was observed in Patient C, associated with a c.1001T>G (p.Leu334Arg) mutation. All affected residues lie in evolutionarily conserved sequence blocks. These additional cases and the associated mutations contribute to an improved appreciation of the variability of this rare skeletal dysplasia. (c) 2010 Wiley-Liss, Inc.
颅骨干骺发育不良(CMD)是一种罕见的硬化性骨骼疾病,由ANKH 基因突变引起,ANKH 编码一种假定的焦磷酸转运膜蛋白。迄今为止,已经描述了六种不同的 ANKH 突变。我们在此报告三例具有 CMD 的单纯性患者的新突变。患者 A 中的 c.1015T>C(p.Cys339Arg)突变与先天性面瘫、早发性传导性听力损失和长骨普遍发育不良有关。患者 B 中的 c.1172T>C(p.Leu391Pro)突变与面瘫、进行性传导性听力损失和管状骨普遍发育不良有关。患者 C 观察到一种较轻的表型,没有颅神经受累,与 c.1001T>G(p.Leu334Arg)突变有关。所有受影响的残基都位于进化保守的序列块中。这些额外的病例和相关突变有助于更好地了解这种罕见骨骼发育不良的变异性。(c)2010 年 Wiley-Liss,Inc.