New clinical findings in oculo-ectodermal syndrome

Clinical Dysmorphology

Volumn 9, Issue 1, 2000, Pages 39-41

  Silengo, Margherita ^a   Lerone, Margherita ^b   Seri, Marco ^b   Priolo, Manuela ^b   Jarre, Laura ^a  

^a UNIVERSITY OF TURIN   (Italy)

^b G GASLINI INSTITUTE   (Italy)

Author keywords

Abnormal hair; Aplasia cutis; Epibulbar dermoids; Macrocephaly; Mental retardation

Indexed keywords

ALOPECIA; ARTICLE; CASE REPORT; HUMAN; MACROCEPHALY; MALE; MENTAL DEFICIENCY; OCULO ECTODERMAL SYNDROME; PRESCHOOL CHILD; PRIORITY JOURNAL; SCALP; SKIN APLASIA; STRABISMUS; TERATOMA;

EID: 0033965856     PISSN: 09628827     EISSN: None     Source Type: Journal    
DOI: 10.1097/00019605-200009010-00008     Document Type: Article

References (5)

1. Evers MEJW, Dijkman-Neerincx RHM, Hamel BCJ (1994). Oculo-Ectodermal syndrome: a new case. Am J Med Genet 53:378-379.
2. Gardner J, Viljoen D (1994). Aplasia cutis congenita with epibulbar dermoids: further evidence for syndromic identity of the ocular ectodermal syndrome. Am J Med Genet 53:317-320.
3. Gorlin RJ, Cohen MM, Levin LS (1990). Syndromes of the head and neck. Oxford University Press: New York. pp. 417-419.
4. Sybert VP (1985). Aplasia cutis congenita: report of 12 new families and review of the literature. Pediatr Dermatol 3:1-14.
5. Toriello HV, Lacassie Y, Droste P, Higgins JV (1993). Provisionally unique ocular and ectodermal defects in two unrelated boys. Am J Med Genet 45:764-766.