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Novel compound heterozygous WDR35 variants in a Chinese patient associated with cranioectodermal dysplasia and ectopic testis: a case report and review of the literature

Abstract Background WDR35 variants are known to cause a rare autosomal recessive disorder-Cranioectodermal dysplasia (CED). The CED patients are commonly present with facial dysmorphisms (frontal bossing and low-set ears), sagittal craniosynostosis, growth retardation, dolichocephaly, skeletal defor...

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Main Authors:	Lijie Li (Author), Cuihua Liu (Author), Ming Tian (Author), Guangbo Li (Author), Jitong Li (Author)
Format:	Book
Published:	BMC, 2023-08-01T00:00:00Z.
Subjects:	article
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