Congenital cataracts facial dysmorphism neuropathy (CCFDN) syndrome: A rare cause of parainfectious rhabdomyolysis

European Journal of Pediatrics

Volumn 166, Issue 7, 2007, Pages 747-749

  Mastroyianni, Sotiria D ^a   Garoufi, Anastasia ^b   Voudris, Konstantinos ^a   Skardoutsou, Angeliki ^b   Stefanidis, Constantinos J ^a   Katsarou, Efstathia ^a   Gooding, Rebecca ^c   Kalaydjieva, Luba ^c  

^a P AND A KYRIAKOU CHILDREN S HOSPITAL   (Greece)

^b UNIVERSITY OF ATHENS   (Greece)

^c UNIVERSITY OF WESTERN AUSTRALIA   (Australia)

Author keywords

CCFDN; Congenital cataracts; Myoglobinuria; Neuropathy; Rhabdomyolysis

Indexed keywords

ALANINE AMINOTRANSFERASE; ASPARTATE AMINOTRANSFERASE; CARNITINE; CREATINE KINASE MB; CREATININE; GLUCOSE; LACTATE DEHYDROGENASE; UREA; URIC ACID;

ALANINE AMINOTRANSFERASE BLOOD LEVEL; ARTICLE; ASPARTATE AMINOTRANSFERASE BLOOD LEVEL; CASE REPORT; CLINICAL FEATURE; CONGENITAL CATARACT FACIAL DYSMORPHISM NEUROPATHY SYNDROME; GENE MUTATION; HUMAN; INFLUENZA VIRUS A; MALE; MUSCLE HYPOTONIA; NERVE CONDUCTION; NEUROLOGIC DISEASE; NONHUMAN; POLYMERASE CHAIN REACTION; PRESCHOOL CHILD; PRIORITY JOURNAL; RHABDOMYOLYSIS; TENDON REFLEX; VIRUS DETECTION;

CATARACT; CHILD, PRESCHOOL; CLUBFOOT; DEVELOPMENTAL DISABILITIES; FACIAL NERVE DISEASES; HUMANS; MALE; MUSCLE HYPOTONIA; PARESIS; REFLEX, ABNORMAL; RHABDOMYOLYSIS; SYNDROME;

EID: 34249024325     PISSN: 03406199     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00431-006-0307-9     Document Type: Article

References (6)

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