Neurological manifestations in individuals with pure cutaneous or syndromic (ruggieri-happle syndrome) phenotypes with "cutis tricolor": A study of 14 cases

Neuropediatrics

Volumn 41, Issue 2, 2010, Pages 60-65

  Lionetti, E ^a   Pavone, P ^b   Kennerknecht, I ^c   Failla, G ^d   Schepis, C ^d   De Pasquale, R ^a   Pavone, L ^a   Ruggieri, M ^a  

^a UNIVERSITY OF CATANIA   (Italy)

^b UNIVERSITY OF CATANIA   (Italy)

^c UNIVERSITY OF MÜNSTER   (Germany)

^d OASI RESEARCH INSTITUTE IRCCS   (Italy)

Author keywords

cutis tricolor; neurology; Ruggieri Happle syndrome

Indexed keywords

PROTEIN ZFHX1B; UNCLASSIFIED DRUG; ZINC FINGER PROTEIN;

ADOLESCENT; ADULT; ARTICLE; CHILD; CLINICAL ARTICLE; CLINICAL FEATURE; CONGENITAL MALFORMATION; CUTIS TRICOLOR; CYTOGENETICS; EEG ABNORMALITY; ELECTROENCEPHALOGRAPHY; FEMALE; GENE DELETION; GENE MUTATION; GENETIC ANALYSIS; HUMAN; MALE; NUCLEAR MAGNETIC RESONANCE IMAGING; PHAKOMATOSIS; PHENOTYPE; PRESCHOOL CHILD; PRIORITY JOURNAL; PSYCHOMOTOR DISORDER; RUGGIERI HAPPLE SYNDROME; SCHOOL CHILD; SEIZURE; SKIN MANIFESTATION;

ADOLESCENT; ADULT; BRAIN; CHILD; CHILD, PRESCHOOL; CHONDRODYSPLASIA PUNCTATA; ELECTROENCEPHALOGRAPHY; FEMALE; HUMANS; MAGNETIC RESONANCE IMAGING; MALE; NERVOUS SYSTEM DISEASES; NEUROLOGIC EXAMINATION; NEUROPSYCHOLOGICAL TESTS; PHENOTYPE; PIGMENTATION DISORDERS; RETROSPECTIVE STUDIES; SKIN; YOUNG ADULT;

EID: 77956251907     PISSN: 0174304X     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-0030-1261919     Document Type: Article

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