|Color Atlas of Pediatric Dermatology|
Section 11. Genodermatoses
Topics Discussed: focal dermal hypoplasia; genetics and dysmorphology.
Sections: Incontinentia Pigmenti, Cutaneous Expressions of the Wiskott-Aldrich Syndrome, Cutaneous Expressions of Ataxia Telangiectasia, Bloom's Syndrome, Poikiloderma Congenitale (Rothmund-Thomson Syndrome), Cutaneous Expressions of Cockayne's Syndrome, Congenital Ectodermal Dysplasia, Hay-Well's Syndrome (AEC), Pachyonychia Congenita, Dyskeratosis Congenita, Neurofibromatosis (Von Recklinghausen's Disease), Neurofibromatosis (Lisch Nodule), Mucosal Neuroma Syndrome, Tuberous Sclerosis, Buschke-Ollendorf Syndrome, Basal Cell Nevus Syndrome, Xeroderma Pigmentosum.
Excerpt:"This figure shows skin and eye defects that may occur in this syndrome. Note the atrophy on the forehead, the ocular defect in the right eye, and the papillomatous changes on the chin...."
The content above is only an
excerpt. For full access, log into an existing user account below, purchase an annual subscription, or
purchase a short-term subscription to the complete website.
offers pediatrics students,
educators, and practioners access to leading McGraw-Hill texts, interactive imaging
content, exclusive multimedia, and flexible curricular tools.
Timed access to all of AccessPediatrics
24 hours for $29.95
48 hours for $49.95