Holoprosencephaly-polydactyly (pseudotrisomy 13) syndrome: case report and diagnostic criteria.

Sergi, Consolato; Gekas, Jean; Kamnasaran, Deepak

Sergi, Consolato; Gekas, Jean; Kamnasaran, Deepak.

Affiliation

Sergi C; Department of Pathology and Laboratory Medicine, University of Alberta, Edmonton, Alberta, Canada.

Fetal Pediatr Pathol ; 31(5): 315-8, 2012 Oct.

Article in En | MEDLINE | ID: mdl-22432933

Subject(s)

Abnormalities, Multiple/pathology; Chromosome Disorders/diagnosis; Fetal Macrosomia/diagnosis; Hand Deformities, Congenital/diagnosis; Holoprosencephaly/diagnosis; Polydactyly/diagnosis; Trisomy/diagnosis; Abnormalities, Multiple/genetics; Abortion, Eugenic; Adult; Chromosome Banding; Chromosome Disorders/genetics; Chromosomes, Human, Pair 13/genetics; DNA Mutational Analysis; Diagnosis, Differential; Fatal Outcome; Female; Fetal Macrosomia/genetics; Hand Deformities, Congenital/genetics; Holoprosencephaly/genetics; Humans; Male; Mutation; Polydactyly/genetics; Trisomy/genetics; Trisomy 13 Syndrome; Ultrasonography, Prenatal

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Trisomy / Abnormalities, Multiple / Fetal Macrosomia / Hand Deformities, Congenital / Holoprosencephaly / Polydactyly / Chromosome Disorders Type of study: Diagnostic_studies Limits: Adult / Female / Humans / Male Language: En Journal: Fetal Pediatr Pathol Journal subject: PATOLOGIA / PEDIATRIA Year: 2012 Type: Article Affiliation country: Canada

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