Congenital poikiloderma with verruciform hyperkeratosis and bone abnormalities. Variant of Rothmund - Thomson syndrome (type Thomson)

European Journal of Pediatric Dermatology

Volumn 9, Issue 2, 1999, Pages 77-80

  Szalai, S ^a   Szalai, Cs ^a   Torok, E ^a  

^a HEIM PÁL CHILDREN S HOSPITAL   (Hungary)

Author keywords

Congenital poikiloderma; Limb defects; Rothmund Thomson syndrome; Verruciform hyperkeratosis

Indexed keywords

ARTICLE; BONE MALFORMATION; CASE REPORT; CATARACT; EPIDERMODYSPLASIA VERRUCIFORMIS; GENETIC VARIABILITY; HISTOPATHOLOGY; HUMAN; HUMAN CELL; HUMAN TISSUE; HYPERKERATOSIS; KARYOTYPE; MALE; POIKILODERMA; PRESCHOOL CHILD; ROTHMUND THOMSON SYNDROME; SYNDROME DELINEATION;

EID: 0033498460     PISSN: 11227672     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (9)