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一种新的常染色体隐性综合征。全血细胞减少症早发、独特的面部特征、生长发育迟缓。

A new autosomal recessive syndrome. Early onset of pancytopenia, distinct facial features, growth retardation and developmental delay.

作者信息

Al-Batniji F S, Mahmoud M A, Van Dijken P J, Al-Asiri R H, Al-Swaid A F, Al-Marshedy A M

机构信息

Department of Pediatrics, Armed Forces Hospital, PO Box 7897, Riyadh 11159, Kingdom of Saudi Arabia.

出版信息

Saudi Med J. 2001 Dec;22(12):1122-6.

Abstract

The association of dysmorphic features and failure of one or more bone marrow cell lines is well known. Examples are Fanconi's anemia and Diamond-Blackfan anemia. This report describes 3 similarly affected children from consanguineous parents, all showing low birth weight, severe growth retardation, distinct facial features, microcephaly, mental retardation and onset of severe pancytopenia in infancy without increased chromosomal breakage. We conclude that these cases represent a new familial autosomal recessive bone marrow failure syndrome.

摘要

畸形特征与一种或多种骨髓细胞系功能衰竭之间的关联是众所周知的。例如范可尼贫血和钻石-黑范贫血。本报告描述了3名来自近亲父母的情况类似的儿童,他们均表现为低出生体重、严重生长发育迟缓、独特的面部特征、小头畸形、智力迟钝以及婴儿期出现严重全血细胞减少症且染色体断裂未增加。我们得出结论,这些病例代表了一种新的家族性常染色体隐性骨髓衰竭综合征。

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