Hoffman H M, Bastian J F, Bird L M
Division of Rheumatology, Allergy and Immunology, University of California at San Diego, 92093-0635, USA.
Clin Dysmorphol. 2001 Jan;10(1):1-8. doi: 10.1097/00019605-200101000-00001.
We report a 6 year old girl with an isolated humoral immune deficiency and a unique combination of dysmorphic features. Physical findings include microcephaly, micrognathia, sickle shaped eyebrows, hypoplastic alae nasi, thenar hypoplasia, partial 4-5 syndactyly of toes, recessed great toes, anterior anus, and hypoplastic labia minora. Radiographic findings include triphalangeal thumbs and hypoplastic first metatarsals. She has postnatal growth retardation and her development is substantially slower than her twin's. Her clinical course has been complicated by recurrent sinopulmonary infections and pneumococcal bacteraemia. Laboratory evaluation revealed hypogammaglobulinaemia, absent B cells, and a 46,XX karyotype. A review of the literature and the London Dysmorphology Database did not produce any recognizable syndromes that match her constellation of findings. She may represent a unique syndrome of unknown etiology.
我们报告了一名6岁女孩,她患有孤立性体液免疫缺陷,并伴有一系列独特的畸形特征。体格检查发现包括小头畸形、小颌畸形、镰刀形眉毛、鼻翼发育不全、大鱼际发育不全、部分4-5趾并指畸形、拇趾内收、肛门前移和小阴唇发育不全。影像学检查发现包括三节指骨拇指和第一跖骨发育不全。她出生后生长发育迟缓,发育明显比她的双胞胎慢。她的临床病程因反复的鼻窦肺部感染和肺炎球菌菌血症而复杂化。实验室检查显示低丙种球蛋白血症、B细胞缺失以及46,XX核型。对文献和伦敦畸形数据库的检索未发现任何与她的一系列表现相符的可识别综合征。她可能代表一种病因不明的独特综合征。