Amir Achiya Zvi, Horev Gadi, Yacobovich Joanne, Bennett Michael, Tamary Hannah
Pediatric Gastroenterology, Hepatology and Nutrition Clinic, Dana-Dwek Children's Hospital, Tel-Aviv Medical Center, Tel Aviv, Israel.
Department of Radiology, Schneider Children's Medical Center of Israel, Petach Tikva, Israel.
Am J Med Genet A. 2017 Feb;173(2):487-490. doi: 10.1002/ajmg.a.38012. Epub 2016 Oct 19.
The congenital dyserythropoietic anemias (CDAs) are a group of rare genetic disorders characterized by ineffective erythropoiesis and the development of secondary hemochromatosis. Distal limb anomalies are a well-documented though rare feature of congenital dyserythropoietic anemia type I, that have not been reported so far in other types. We describe a patient with congenital dyserythropoietic anemia type II and four members of a family with clinical features of congenital dyserythropoietic anemia type III with distal limb anomalies. The patient with congenital dyserythropoietic anemia type II presented with bilateral complete osseous syndactyly of the hands, and bilateral complete cutaneous syndactyly of feet. Three of the four affected family members with congenital dyserythropoietic anemia type III had partial absence of fingers, small or absent nails, overlapping toes, and short metatarsals. We suggest that similar to congenital dyserythropoietic anemia type I, distal anomalies may appear in some patients with congenital dyserythropoietic anemia types II and III. Patients presenting with anemia and distal limb anomalies should be further investigated for the presence of congenital dyserythropoietic anemia. © 2016 Wiley Periodicals, Inc.
先天性红细胞生成异常性贫血(CDAs)是一组罕见的遗传性疾病,其特征为红细胞生成无效和继发性血色素沉着症的发生。远端肢体异常是I型先天性红细胞生成异常性贫血的一个虽罕见但有充分文献记载的特征,迄今为止在其他类型中尚未见报道。我们描述了一名II型先天性红细胞生成异常性贫血患者以及一个有III型先天性红细胞生成异常性贫血临床特征并伴有远端肢体异常的家族中的四名成员。该II型先天性红细胞生成异常性贫血患者表现为双手双侧完全骨性并指以及双足双侧完全皮肤并指。四名患有III型先天性红细胞生成异常性贫血的受影响家族成员中有三名存在部分手指缺如、指甲小或无指甲、足趾重叠以及跖骨短。我们认为,与I型先天性红细胞生成异常性贫血类似,远端异常可能出现在一些II型和III型先天性红细胞生成异常性贫血患者中。对于出现贫血和远端肢体异常的患者,应进一步检查是否存在先天性红细胞生成异常性贫血。© 2016威利期刊公司