Expanding the known phenotype of Mullegama-Klein-Martinez syndrome in male patients.

Expanding the known phenotype of Mullegama-Klein-Martinez syndrome in male patients.
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DOI:
10.1038/s41439-021-00169-3
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发表时间:
2021-09-27
影响因子:
1.5
通讯作者:
Nagy V
Nagy V
中科院分区:
其他
文献类型:
--
作者:
Freyberger F;Kokotović T;Krnjak G;Frković SH;Nagy V

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在这里,我们报告了一个新的情况下,男性患者的半合子错义变异STAG 2(p.Tyr159His)导致Mullegama-Klein-Martinez综合征(MKMS),一种罕见的X连锁粘连蛋白病。他与先前报道的携带STAG 2变体p.Tyr159Cys的男性患者具有不同的临床特征,表明这种表型是由突变的位置决定的。此外,我们的患者表现出以前与MKMS无关的症状,扩展了这种罕见疾病的已知临床表型。
Here, we report a novel case of a male patient with a hemizygous missense variant in STAG2 (p.Tyr159His) resulting in Mullegama–Klein–Martinez syndrome (MKMS), a rare X-linked cohesinopathy. He shares distinct clinical features with a previously reported male patient carrying the STAG2 variant p.Tyr159Cys, suggesting that this phenotype is determined by the position of the mutation. Additionally, our patient exhibits symptoms not previously associated with MKMS, expanding the known clinical phenotype of this rare disease.
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