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Report of a novel UBA2 variant causing Aplasia Cutis Congenita with Ectrodactyly syndrome (ACCES) in an Indian family.

ABSTRACT:

SUBMITTER: Shirodkar AN 

PROVIDER: S-EPMC7617595 | biostudies-literature | 2025 Jul

REPOSITORIES: biostudies-literature

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Report of a novel UBA2 variant causing Aplasia Cutis Congenita with Ectrodactyly syndrome (ACCES) in an Indian family.

Shirodkar Aditi Nilesh AN   Akhil K A KA   Bhat Vivekananda V   Shah Hitesh H   Shukla Anju A   Periyasamy Radhakrishnan R  

Clinical dysmorphology 20250528 3

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