Wrinkly skin syndrome [12]

Clinical and Experimental Dermatology

Volumn 30, Issue 5, 2005, Pages 590-592

  Hamamy, H ^a   Masri, A ^b   Ajlouni, K ^a  

^a National Center for Diabetes Endocrinology and Genetics Jordan   (Jordan)

^b JORDAN UNIVERSITY HOSPITAL   (Jordan)

Author keywords

[No Author keywords available]

Indexed keywords

ANTERIOR FONTANEL; BRACHYCEPHALY; CASE REPORT; CHROMOSOME ANALYSIS; CLINICAL FEATURE; CONGENITAL SKIN DISEASE; DEVELOPMENTAL DISORDER; ELECTROPHYSIOLOGY; EVOKED VISUAL RESPONSE; FACE DYSMORPHIA; FEMALE; HUMAN; HYPOTELORISM; INTRACRANIAL PRESSURE; LETTER; NERVE CONDUCTION; NUCLEAR MAGNETIC RESONANCE; PRESCHOOL CHILD; PRIORITY JOURNAL; SYNDROME;

ABNORMALITIES, MULTIPLE; CHILD, PRESCHOOL; CRANIOFACIAL ABNORMALITIES; CUTIS LAXA; FEMALE; HUMANS; SYNDROME;

EID: 23044480059     PISSN: 03076938     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1365-2230.2005.01825.x     Document Type: Letter

References (5)

1. Gazit E, Goodman RM, Katznelson M, Rotem Y. The wrinkly skin syndrome: a new heritable disorder of connective tissue. Clin Genet 1973; 4: 186-92.
2. Kreuz FR, Wittwer BH. Del (2q) - cause of the wrinkly skin syndrome? Clin Genet 1993; 43: 132-8.
3. Boente M, Winik B, Asial R. Wrinkly skin syndrome: ultrastructural alterations of the elastic fibers. Pediatric Dermatol 1999; 16: 113-7.
4. Al-Gazali L, Sztriha L, Skaff F, Haas D. Gerodermia osteodysplastica and wrinkly skin syndrome: are they the same? Am J Med Genet 2001; 101: 213-20.
5. Zlotogora J. Wrinkly skin syndrome and the syndrome of cutis laxa with growth and developmental delay represent the same disorder. Am J Med Genet 1999; 85: 195.