Cutis laxa with growth and developmental delay [2]

Clinical Pediatrics

Volumn 40, Issue 7, 2001, Pages 422-423

  Karakurt, C ^a   Sipahi, T ^a   Ceylaner, S ^a   Senocak F ^a   Karademir, S ^a   Becer, M ^a  

^a DR SAMI ULUS CHILDREN S HOSPITAL   (Turkey)

Author keywords

[No Author keywords available]

Indexed keywords

AUTOSOMAL DOMINANT DISORDER; CARDIOVASCULAR SYSTEM; CASE REPORT; CHILD; CLINICAL FEATURE; CUTIS LAXA; DEVELOPMENTAL DISORDER; FEMALE; GROWTH RETARDATION; HUMAN; INFANT; LETTER; PHOTOGRAPHY; PHYSICAL EXAMINATION;

EID: 0034932642     PISSN: 00099228     EISSN: None     Source Type: Journal    
DOI: 10.1177/000992280104000715     Document Type: Letter

References (5)

1. Autosomal recessive cutis laxa syndrome
2. An elastin gene mutation producing abnormal tropoelastin and abnormal elastic fibres in a patient with autosomal dominant cutis laxa
3. Syndrome of cutis laxa, ligamentous laxity and delayed development
4. Cutis laxa with intrauterine growth retardation and hip dislocation in a male
5. Congenital cutis laxa with retardation of growth and development