A prospective observational study of associated anomalies in Hirschsprung's disease

Orphanet Journal of Rare Diseases

Volumn 8, Issue 1, 2013, Pages

  Pini Prato, Alessio ^a   Rossi, Valentina ^a,b   Mosconi, Manuela ^a   Holm, Catarina ^a   Lantieri, Francesca ^b   Griseri, Paola ^a   Ceccherini, Isabella ^a   Mavilio, Domenico ^c,d   Jasonni, Vincenzo ^a   Tuo, Giulia ^a   Derchi, Maria ^a   Marasini, Maurizio ^a   Magnano, Gianmichele ^a   Granata, Claudio ^a   Ghiggeri, Gianmarco ^a   Priolo, Enrico ^a   Sposetti, Lorenza ^a   Porcu, Adelina ^a   Buffa, Piero ^a   Mattioli, Girolamo ^a,b  

^a G GASLINI INSTITUTE   (Italy)

^b UNIVERSITY OF GENOA   (Italy)

^c HUMANITAS CLINICAL AND RESEARCH CENTER   (Italy)

^d UNIVERSITY OF MILAN   (Italy)

Author keywords

Associated anomalies; Hirschsprung; Observational study; Phenotype

Indexed keywords

AGANGLIONOSIS; ARTICLE; AUDIOMETRY; CENTRAL NERVOUS SYSTEM MALFORMATION; CHILD; CHROMOSOME ABERRATION; CLINICAL ARTICLE; CLINICAL FEATURE; CONGENITAL HEART DISEASE; CONGENITAL MALFORMATION; FEMALE; GENETIC SCREENING; HEARING IMPAIRMENT; HIRSCHSPRUNG DISEASE; HOSPITAL ADMISSION; HUMAN; INFANT; INFORMED CONSENT; KIDNEY MALFORMATION; MALE; MEDICAL SPECIALIST; OBSERVATIONAL STUDY; PHENOTYPE; PRESCHOOL CHILD; PROSPECTIVE STUDY; SCHOOL CHILD; SEX DIFFERENCE; URINARY TRACT MALFORMATION; VISUAL IMPAIRMENT; ADOLESCENT; ADULT; PATHOLOGY; YOUNG ADULT;

ADOLESCENT; ADULT; CHILD; CHILD, PRESCHOOL; FEMALE; HIRSCHSPRUNG DISEASE; HUMANS; INFANT; MALE; PHENOTYPE; PROSPECTIVE STUDIES; YOUNG ADULT;

EID: 84887855619     PISSN: None     EISSN: 17501172     Source Type: Journal    
DOI: 10.1186/1750-1172-8-184     Document Type: Article

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