| Literature DB >> 31961058 |
Sarah E Sheppard1, Anna Smith2, Katheryn Grand1, Jennifer Pogoriler3,4, Adam I Rubin2,3,4,5, Erica Schindewolf6, Mark P Fitzgerald7, Julie Moldenhauer6, Pablo Laje6,8, William Peranteau6,8, Elizabeth Bhoj1,4, Patrick McMahon2,4, Leslie Castelo-Soccio2,4.
Abstract
Nevus comedonicus syndrome (NCS) is a rare epidermal nevus syndrome characterized by ocular, skeletal, and central nervous system anomalies. We present a 23-month-old boy with a history of a congenital pulmonary airway malformation (CPAM) of the lung and a congenital cataract who developed progressive linear and curvilinear plaques of dilated follicular openings with keratin plugs (comedones) on parts of his scalp, face, and body consistent with nevus comedonicus. MRI of the brain demonstrated an aneurysm of the right internal carotid artery. Genetic testing identified NEK9 c.1755_1757del (p.Thr586del) at mean allele frequency of 28% in the nevus comedonicus. This same mutation was present in the CPAM tissue. This is the first case of a CPAM in a patient with an epidermal nevus syndrome. This case expands the phenotype of nevus comedonicus syndrome to include CPAM and vascular anomalies.Entities:
Keywords: NEK9; congenital pulmonary airway malformation of the lung; epidermal nevus; nevus comedonicus
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Year: 2020 PMID: 31961058 DOI: 10.1002/ajmg.a.61490
Source DB: PubMed Journal: Am J Med Genet A ISSN: 1552-4825 Impact factor: 2.802