The Hoyeraal-Hreidarsson syndrome: The fourth case of a separate entity with prenatal growth retardation, progressive pancytopenia and cerebellar hypoplasia

European Journal of Pediatrics

Volumn 154, Issue 4, 1995, Pages 304-308

  Aalfs, Cora M ^a   van den Berg, Henk ^a   Barth, Peter G ^a   Hennekam, Raoul C M ^a  

^a ACADEMIC MEDICAL CENTER   (Netherlands)

Author keywords

Autosomal recessive inheritance; Cerebellar hypoplasia; Developmental delay; Growth retardation; Panoytopenia

Indexed keywords

ARTICLE; CASE REPORT; CEREBELLUM HYPOPLASIA; DEVELOPMENTAL DISORDER; HEREDITY; HOYERAAL HREIDARSSON SYNDROME; HUMAN; INTRAUTERINE GROWTH RETARDATION; MALE; MICROCEPHALY; PANCYTOPENIA; PRIORITY JOURNAL; SYNDROME DELINEATION;

ABNORMALITIES, MULTIPLE; CASE REPORT; CEREBELLUM; CHILD, PRESCHOOL; CHROMOSOME ABERRATIONS; CHROMOSOME DISORDERS; FETAL GROWTH RETARDATION; FOLLOW-UP STUDIES; GENES, RECESSIVE; HUMAN; INFANT; INFANT, NEWBORN; MAGNETIC RESONANCE IMAGING; MALE; PANCYTOPENIA; SEX CHROMOSOME ABERRATIONS; SYNDROME; X CHROMOSOME;

EID: 0028916022     PISSN: 03406199     EISSN: 14321076     Source Type: Journal    
DOI: 10.1007/BF01957367     Document Type: Article

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