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A new autosomal recessive syndrome. Early onset of pancytopenia, distinct facial features, growth retardation and developmental delay

Authors :
F S, Al-Batniji
M A, Mahmoud
P J, Van Dijken
R H, Al-Asiri
A F, Al-Swaid
A M, Al-Marshedy
Source :
Saudi medical journal. 22(12)
Publication Year :
2002

Abstract

The association of dysmorphic features and failure of one or more bone marrow cell lines is well known. Examples are Fanconi's anemia and Diamond-Blackfan anemia. This report describes 3 similarly affected children from consanguineous parents, all showing low birth weight, severe growth retardation, distinct facial features, microcephaly, mental retardation and onset of severe pancytopenia in infancy without increased chromosomal breakage. We conclude that these cases represent a new familial autosomal recessive bone marrow failure syndrome.

Details

ISSN :
03795284
Volume :
22
Issue :
12
Database :
OpenAIRE
Journal :
Saudi medical journal
Accession number :
edsair.pmid..........cff64fba798366febff3835828682a6d