Linear facial skin defects associated with microphthalmia and other malformations, with chromosome deletion Xp22.1

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Bibliographic Details
Published inJournal of the American Academy of Dermatology Vol. 31; no. 4; pp. 680 - 682
Main Authors Eng, Ana, Lebel, Robert Roger, Elejalde, B. Rafael, Anderson, Craig, Bennett, Larry
Format Journal Article
LanguageEnglish
Published New York, NY Mosby, Inc 01.10.1994
Elsevier
Subjects
Abnormalities, Multiple - pathology
Biological and medical sciences
Chromosome aberrations
Chromosome Deletion
Ear, External - abnormalities
Facial Bones - abnormalities
Facial Dermatoses - complications
Facial Dermatoses - pathology
Female
Humans
Infant
Infant, Newborn
Medical genetics
Medical sciences
Microphthalmos - complications
Microphthalmos - pathology
Syndrome
X Chromosome
Chromosomal aberration
Human
Skin disease
Agenesis
Abnormal X chromosome
Congenital disease
Case study
Eye disease
Association
Newborn
Malformation
Deletion
Abnormal chromosome
Skin
Face
Microphthalmia
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Bibliography:ObjectType-Case Study-2
SourceType-Scholarly Journals-1
ObjectType-Feature-4
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ObjectType-Report-1
ObjectType-Article-3
ISSN:0190-9622
1097-6787
DOI:10.1016/S0190-9622(08)81743-4