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Urticaria pigmentosa in a child with Prader-Labhart-Willi syndrome

✍ Scribed by Fowler, Jr., Joseph F.; Butler, Merlin G.

Book ID
123084922
Publisher
Elsevier Science
Year
1989
Tongue
English
Weight
240 KB
Volume
21
Category
Article
ISSN
1097-6787

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A 16-year-old boy with Prader-Labhart-Willi syndrome (PLWS) had hypotonia, feeding difficulties, failure to thrive, strabismus and bilateral inguinal hernias with cryptorchidism during infancy followed by hyperphagia, marked early-onset obesity with insulin-dependent diabetes mellitus and necrobiosi