
Kin with no skin: Johanson–Blizzard syndrome in siblings: A rare association of aplasia cutis congenita
Author(s) -
GS Asha,
K Kavya Shree,
T N Revathi,
Kanathur Shilpa
Publication year - 2021
Publication title -
indian journal of paediatric dermatology
Language(s) - English
Resource type - Journals
eISSN - 2319-7269
pISSN - 2319-7250
DOI - 10.4103/ijpd.ijpd_172_20
Subject(s) - aplasia cutis congenita , ectodermal dysplasia , medicine , aplasia , scalp , congenital disorder , cutis , dermatology , ubiquitin ligase , cutis laxa , failure to thrive , genetic disorder , pathology , anatomy , genetics , gene , pediatrics , disease , surgery , biology , ubiquitin