 |  | Color Atlas of Pediatric DermatologySection 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...."
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