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Ulerythema ophryogenes with multiple congenital anomalies

✍ Scribed by Burnett, Joseph W.; Schwartz, Marcia F.; Berberian, Brenda J.

Book ID
122954701
Publisher
Elsevier Science
Year
1988
Tongue
English
Weight
768 KB
Volume
18
Category
Article
ISSN
1097-6787

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We present a patient with partial monosomy of the short arm of chromosome 18 caused by de novo translocation t(Y;18) and a generalized form of keratosis pilaris (keratosis pilaris affecting the skin follicles of the trunk, limbs and face-ulerythema ophryogenes). Two-color FISH with centromerespecifi