Van Maldergem L, Siitonen H A, Jalkh N, Chouery E, De Roy M, Delague V, Muenke M, Jabs E W, Cai J, Wang L L, Plon S E, Fourneau C, Kestilä M, Gillerot Y, Mégarbané A, Verloes A
Centre de Génétique Humaine, Institut de Pathologie et de Génétique, Loverval, Belgium.
J Med Genet. 2006 Feb;43(2):148-52. doi: 10.1136/jmg.2005.031781. Epub 2005 Jun 17.
Baller-Gerold syndrome (BGS) is a rare autosomal recessive condition with radial aplasia/hypoplasia and craniosynostosis (OMIM 218600). Of >20 cases reported so far, a few appear atypical and have been reassigned to other nosologic entities, including Fanconi anaemia, Roberts SC phocomelia, and Pfeiffer syndromes after demonstration of corresponding cytogenetic or molecular abnormalities. Clinical overlap between BGS, Rothmund-Thomson syndrome (RTS), and RAPADILINO syndrome is noticeable. Because patients with RAPADILINO syndrome and a subset of patients with RTS have RECQL4 mutations, we reassessed two previously reported BGS families and found causal mutations in RECQL4 in both. In the first family, four affected offspring had craniosynostosis and radial defect and one of them developed poikiloderma. In this family, compound heterozygosity for a R1021W missense mutation and a g.2886delT frameshift mutation of exon 9 was found. In the second family, the affected male had craniosynostosis, radial ray defect, poikiloderma, and short stature. He had a homozygous splice site mutation (IVS17-2A>C). In both families, the affected offspring had craniosynostosis, radial defects, and growth retardation, and two developed poikiloderma. Our results confirm that BGS in a subgroup of patients is due to RECQL4 mutations and could be integrated into a clinical spectrum that encompasses RTS and RAPADILINO syndrome.
巴勒-杰罗尔德综合征(BGS)是一种罕见的常染色体隐性疾病,伴有桡骨发育不全/发育不良和颅缝早闭(OMIM 218600)。在迄今报道的20多例病例中,有几例表现不典型,在证实存在相应的细胞遗传学或分子异常后,已被重新归类到其他疾病实体,包括范可尼贫血、罗伯茨短肢侏儒综合征和 Pfeiffer 综合征。BGS、罗思蒙德-汤姆森综合征(RTS)和RAPADILINO综合征之间的临床重叠很明显。由于RAPADILINO综合征患者和一部分RTS患者存在RECQL4突变,我们重新评估了两个先前报道的BGS家系,发现两个家系中均存在RECQL4致病突变。在第一个家系中,四名患病后代患有颅缝早闭和桡骨缺陷,其中一人出现了皮肤异色症。在这个家系中,发现外显子9存在R1021W错义突变和g.2886delT移码突变的复合杂合性。在第二个家系中,患病男性患有颅缝早闭、桡骨射线缺陷、皮肤异色症和身材矮小。他有一个纯合剪接位点突变(IVS17-2A>C)。在两个家系中,患病后代均患有颅缝早闭、桡骨缺陷和生长发育迟缓,两人出现了皮肤异色症。我们的结果证实,一部分患者的BGS是由RECQL4突变引起的,并且可以纳入一个包含RTS和RAPADILINO综合征的临床谱系中。