Ritscher-Schinzel or 3C syndrome, with heterochromatic iris

Pediatrics International

Volumn 45, Issue 5, 2003, Pages 574-576

  Hatzidaki, Eleftheria ^a   Manoura, Antonia ^a   Korakaki, Eftychia ^a   Germanakis, John ^a   Karabekios, Spyros ^a   Giannakopoulou, Christina ^a,b  

^a UNIVERSITY OF CRETE   (Greece)

^b NONE   (Greece)

Author keywords

[No Author keywords available]

Indexed keywords

ABDOMINAL RADIOGRAPHY; ANAMNESIS; ARTICLE; BONE RADIOGRAPHY; BRAIN RADIOGRAPHY; CASE REPORT; CEREBELLUM HYPOPLASIA; CEREBELLUM VERMIS; CLINICAL FEATURE; CRANIO CEREBELLO CARDIAC SYNDROME; DANDY WALKER SYNDROME; DIAGNOSTIC PROCEDURE; DISEASE COURSE; ECHOCARDIOGRAPHY; HEART ATRIUM SEPTUM DEFECT; HUMAN; IRIS DISEASE; LABORATORY TEST; MALE; NEWBORN; NUCLEAR MAGNETIC RESONANCE IMAGING; PATENT DUCTUS ARTERIOSUS; PHENOTYPE; PHYSICAL EXAMINATION; PRIORITY JOURNAL; RITSCHER SCHINZEL SYNDROME; SKULL DEFECT; TESTIS DISEASE;

ABNORMALITIES, MULTIPLE; CEREBELLUM; CRYPTORCHIDISM; DANDY-WALKER SYNDROME; HEART DEFECTS, CONGENITAL; HUMANS; INFANT, NEWBORN; IRIS DISEASES; MALE; SKULL; SYNDROME;

EID: 0242408383     PISSN: 13288067     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1442-200X.2003.01789.x     Document Type: Article

References (13)

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