Spectrum of skeletal abnormalities in a complex malformation syndrome with "cutis tricolor" (Ruggieri-Happle syndrome)

Acta Paediatrica, International Journal of Paediatrics

Volumn 100, Issue 1, 2011, Pages 121-127

  Ruggieri, Martino ^a   Roggini, Mario ^b   Kennerknecht, Ingo ^c   Polizzi, Agata ^d   Distefano, Angela ^e   Pavone, Vito ^a  

^a UNIVERSITY OF CATANIA   (Italy)

^b SAPIENZA UNIVERSITY OF ROME   (Italy)

^c UNIVERSITY OF MÜNSTER   (Germany)

^d National Centre for Rare Diseases   (Italy)

^e INSTITUTE OF NEUROLOGICAL SCIENCES   (Italy)

Author keywords

Cutis tricolor; Ruggieri Happle syndrome; Skeletal dysplasia

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; ATLAS; CHILD; CLINICAL ARTICLE; CUTIS TRICOLOR; FEMALE; FRONTAL BOSSING; HUMAN; HYPERPIGMENTATION; HYPOPIGMENTATION; KYPHOSIS; LORDOSIS; MALE; MALFORMATION SYNDROME; PRESCHOOL CHILD; PRIORITY JOURNAL; PROGNATHIA; SCHOOL CHILD; SCOLIOSIS; SELLA TURCICA; SKELETON MALFORMATION; SKIN DEFECT; SKIN MANIFESTATION;

ABNORMALITIES, MULTIPLE; ADOLESCENT; ADULT; BIOLOGICAL MARKERS; BONE AND BONES; CHILD; CHILD, PRESCHOOL; FEMALE; HUMANS; MALE; PHENOTYPE; PIGMENTATION DISORDERS; PROSPECTIVE STUDIES; RETROSPECTIVE STUDIES; SYNDROME; YOUNG ADULT;

EID: 78650119966     PISSN: 08035253     EISSN: 16512227     Source Type: Journal    
DOI: 10.1111/j.1651-2227.2010.01970.x     Document Type: Article

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