Open AccessPallister–Killian syndrome in a two‐year‐old boy
Author(s) -
Stone Leigh,
Tripuraneni Ramya,
Bain Michelle,
Hernandez Claudia
Publication year - 2017
Publication title -
clinical case reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.21
H-Index - 9
ISSN - 2050-0904
DOI - 10.1002/ccr3.892
Subject(s) - medicine , pediatrics
Key Clinical Message Pallister–Killian syndrome ( PKS ) is a rare, sporadic, multisystem developmental disorder characterized by craniofacial dysmorphic features. We report a case of a two‐year‐old boy with PKS to highlight the cutaneous findings and emphasize the importance of diagnostic skin biopsies in patients with cutaneous pigmentation changes and distinctive facial features.