唇腭裂伴TAR综合征1例报道

A. Naseh, A. Hafizi, F. Malek, H. Mozdarani, V. Yassaee
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引用次数: 5

摘要

TAR(血小板减少-桡骨缺失)是一种临床定义的综合征,其特征是少核细胞性血小板减少和双侧拇指桡骨缺失。我们描述一个女性新生儿作为一个罕见的病例TAR综合征与口面裂。患者骨髓穿刺显示骨髓巨核细胞明显减少。我们的临床观察与TAR综合征一致。然而,其他唇腭裂和桡骨发育不全的综合征,如Roberts综合征(四足畸形)、Edwards综合征和Fanconi和sc型phocomelia(肢体减少程度较小),应考虑。我们的细胞遗传学研究排除了其他重叠染色体综合征。RBM8A分析可显示核苷酸改变,从而明确诊断。我们的目的是将这种唇裂和腭裂加入到有关TAR综合征的文献中。- Eva Klopocki, Harald Schulz, Gabriele Straub,Judith Hall,Fabienne Trotier等(2007年2月);在血小板减少-桡骨缺失综合征中涉及微缺失的复杂遗传模式类似于常染色体隐性遗传。美国人类遗传学杂志80:232-240
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TAR Syndrome, a Rare Case Report with Cleft Lip/Palate
TAR (Thrombocytopenia-Absent Radius) is a clinicallydefined syndrome characterized by hypomegakarocytic thrombocytopenia and bilateral absence of radius in the presence of both thumbs . We describe a female neonate as a rare case of TAR syndrome with orofacial cleft. Bone marrow aspiration of the patient revealed a cellular marrow with marked reduction of megakaryocytes. Our clinical observation is consistent with TAR syndrome. However, other syndromes with cleft lip/palate and radial aplasia like Roberts syndrome (tetraphocomelia), Edwards syndrome and Fanconi and sc phocomelia (which has less degree of limb reduction) should be considered. Our cytogenetic study excludes other overlapping chromosomal syndromes. RBM8A analysis may reveal nucleotide alteration, leading to definite diagnosis. Our objective is adding this cleft lip and cleft palate to the literature regarding TAR syndrome. - Eva Klopocki, Harald Schulz, Gabriele Straub,Judith Hall,Fabienne Trotier, et al(February 2007) ;Complex inheritance pattern Resembeling Autosomal Recessive Inheritance Involving a Microdeletion in Thrombocytopenia-Absent Radius Syndrome.The American Journal of Human Genetics 80:232-240
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