RT Journal Article
SR Electronic
T1 Syndrome of Cutis Laxa Ligamentous Laxity and Delayed Development
JF Pediatrics
JO Pediatrics
FD American Academy of Pediatrics
SP 850
OP 856
VO 72
IS 6
A1 Sakati, Nadia O.
A1 Nyhan, William L.
A1 Shear, Carol S.
A1 Kattan, Hoda
A1 Akhtar, Mohamed
A1 Bay, Carolyn
A1 Jones, Kenneth Lyons
A1 Schackner, Lawrence
YR 1983
UL http://pediatrics.aappublications.org/content/72/6/850.abstract
AB Congential cutis laxa with ligamentous laxity and delayed development appears to be a distinct syndrome. Experience with six patients brings the total number of cases described to 13. Characteristics of the syndrome include congenital dislocation of the hips, wide patency and delayed closure of the anterior fontanel, and delayed intrauterine growth and extrauterine growth and development. Each of the 13 patients has been female. Inheritance may be as an autosomal recessive or an X-linked dominant lethal in the male.