ABSTRACT
We report on a 34-week-old infant with restrictive dermopathy (RD), a rare lethal
genodermatosis, characterized by an abnormal skin growth and differentiation with
thin, tightly adherent skin that causes a dysmorphic face, generalized flexion joint
contractures, and respiratory insufficiency. Kaplan-Meier analysis of 32 previously
well-described infants affected with RD showed a median survival of 132 hours. Lethal
congenital contractural syndromes, including Pena-Shokeir phenotype, cerebro-oculo
facio-skeletal syndrome, and lethal multiple pterygium syndrome, should be considered
first in the differential diagnosis. Other lethal contractural syndromes are discussed.
KEYWORD
Restrictive dermopathy - differential diagnosis - congenital disorder