Persistent congenital milia involving the skin of the whole body in an infant with trisomy 13 syndrome.

Abstract	Milia are tiny pearly-white cysts on the surface of the skin. In newborns, milia are usually located around the nose and eyes and generally disappear after the first several weeks of life. Trisomy 13 is a severe chromosomal disorder, with various complications. Here, we report a case of a 9-month-old female infant with trisomy 13 who had persistent congenital milia covering her entire body surface.
Authors	Noriaki Nakai, Yasutaro Okuzawa, Norito Katoh, Saburo Kishimoto
Journal	Pediatric dermatology (Pediatr Dermatol) Vol. 27 Issue 6 Pg. 657-8 ( 2010) ISSN: 1525-1470 [Electronic] United States
PMID	21510019 (Publication Type: Case Reports, Journal Article)
Copyright	© 2010 Wiley Periodicals, Inc.
Topics	Biopsy Chromosome Disorders (complications) Chromosomes, Human, Pair 13 Epidermal Cyst (complications, pathology) Female Humans Infant Severity of Illness Index Trisomy Trisomy 13 Syndrome

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