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AKT3 中的镶嵌性致病变体导致毛细血管畸形和发育不良。

Mosaic pathogenic variants in AKT3 cause capillary malformation and undergrowth.

机构信息

Comprehensive Vascular Anomaly Program, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.

Department of Physical Therapy, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.

出版信息

Am J Med Genet A. 2023 May;191(5):1442-1446. doi: 10.1002/ajmg.a.63121. Epub 2023 Jan 25.

Abstract

Capillary malformations are slow-flow vascular malformations that affect the microcirculation including capillaries and post capillary venules and can be associated with growth differences. Specifically, the association of capillary malformations with undergrowth is a vastly understudied vascular syndrome with few reports of genetic causes including PIK3CA, GNAQ, and GNA11. Recently, a somatic pathogenic variant in AKT3 was identified in one child with a cutaneous vascular syndrome similar to cutis marmorata telangiectatica congenita, undergrowth, and no neurodevelopmental features. Here, we present a male patient with a capillary malformation and undergrowth due to a somatic pathogenic variant in AKT3 to confirm this association. It is essential to consider that mosaic pathogenic variants in AKT3 can cause a wide spectrum of disease. There is a need for future studies focusing on capillary malformations with undergrowth to understand the underlying mechanism.

摘要

毛细血管畸形是一种低流速的血管畸形,影响微循环,包括毛细血管和后毛细血管小静脉,并可能与生长差异有关。具体来说,毛细血管畸形与发育不良的关联是一种研究甚少的血管综合征,仅有少数关于遗传原因的报道,包括 PIK3CA、GNAQ 和 GNA11。最近,在一名患有类似于先天性大理石样皮肤毛细血管扩张症、发育不良且无神经发育特征的皮肤血管综合征的儿童中,发现了 AKT3 的体细胞致病性变异。在此,我们介绍了一名男性患者,其毛细血管畸形和发育不良是由于 AKT3 的体细胞致病性变异引起的,以证实这种关联。必须考虑到 AKT3 的镶嵌性致病性变异可引起广泛的疾病。需要进一步研究关注伴有发育不良的毛细血管畸形,以了解潜在的机制。

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