Cohen syndrome coincident with epidermolytic palmoplantar keratoderma caused by novel KRT9 gene mutation: A rare case report. | MediFind

Cohen syndrome coincident with epidermolytic palmoplantar keratoderma caused by novel KRT9 gene mutation: A rare case report.

Journal: Asian Journal Of Surgery

Published: July 31, 2023

Authors

Yanping Shu, Yongzhe Hou, Qin Zhang

Relevant Conditions

Microcephaly, Achalasia Microcephaly Syndrome, Hypotonia, Palmoplantar Keratoderma, Acrokeratoelastoidosis of Costa, Obesity, Cortical Dysplasia, Late-Onset Retinal Degeneration, Epidermolytic Palmoplantar Keratoderma, Cohen Syndrome, Nearsightedness

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