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Anew autosomal recessive syndrome. early onset of pancytopenia, distinct facial features, growth retardation and developmental delay
Saudi Medical Journal. 2001; 22 (12): 1122-1126
in English | IMEMR | ID: emr-58228
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
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Index: IMEMR (Eastern Mediterranean) Main subject: Pancytopenia / Bone Marrow / Child / Developmental Disabilities / Face / Growth / Genetic Diseases, Inborn / Intellectual Disability Type of study: Case report Limits: Female / Humans / Male Language: English Journal: Saudi Med. J. Year: 2001

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Index: IMEMR (Eastern Mediterranean) Main subject: Pancytopenia / Bone Marrow / Child / Developmental Disabilities / Face / Growth / Genetic Diseases, Inborn / Intellectual Disability Type of study: Case report Limits: Female / Humans / Male Language: English Journal: Saudi Med. J. Year: 2001