Multidisciplinary team approach in harlequin baby a case report

Harlequin ichthyosis [HI] is an autosomal recessive disorder with a mortality rate of 44%. HI is caused by a homozygous mutation in a protein adenosine triphosphate binding cassette subfamily A member 12. We present a case of HI in one of two dizygotic twins successfully managed using a multidisciplinary approach and discharged from the hospital at day 65 of life