Dabir Tabib, Sills A M, Hall Christine M, Bennett Chris, Wilson Louise C, Hennekam Raoul C M
Clinical and Molecular Genetics Unit, Institute of Child Health and Great Ormond Street Hospital for Children, UCL, London Department of Paediatrics, Huddersfield Royal Infirmary, Lindley, Huddersfield, UK Yorkshire Regional Genetics Service, St James's University Hospital, Leeds Department of Paediatrics, Academic Medical Centre, Amsterdam, The Netherlands.
Clin Dysmorphol. 2007 Jul;16(3):197-201. doi: 10.1097/MCD.0b013e32801470d8.
Primary hypertrophic osteoarthropathy is a condition characterized by clubbing, arthropathy and periostosis of long tubular bones. Three variants of primary hypertrophic osteoarthropathy are distinguished: pachydermoperiostosis, which shows as additional symptom pachydermia; cranio-osteoarthropathy, which has a decreased neurocranium ossification as additional feature; and a secondary form. Primary hypertrophic osteoarthropathy is also genetically heterogeneous, with evidence for both autosomal dominant and autosomal recessive inheritance. We describe two sibs with cranio-osteoarthropathy and briefly review previously reported cases. The present cases demonstrate the phenotypic variability of the condition. The consanguinity in the present family and analysis of previously described cases support autosomal recessive inheritance for cranio-osteoarthropathy.
原发性肥厚性骨关节病是一种以杵状指、关节病和长管状骨骨膜增生为特征的疾病。原发性肥厚性骨关节病可分为三种类型:厚皮性骨膜病,其表现为额外的厚皮症状;颅骨骨关节病,其具有颅骨骨化减少这一额外特征;以及继发性形式。原发性肥厚性骨关节病在遗传上也具有异质性,有常染色体显性和常染色体隐性遗传的证据。我们描述了两名患有颅骨骨关节病的同胞,并简要回顾了先前报道的病例。目前的病例证明了该疾病的表型变异性。本家族中的近亲关系以及对先前描述病例的分析支持颅骨骨关节病的常染色体隐性遗传。