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Arch Med Res ; 32(4): 318-23, 2001.
Article in English | MEDLINE | ID: mdl-11440791

ABSTRACT

Shwachman-Diamond Syndrome (SDS) is an inherited condition with multisystemic abnormalities including pancreatic exocrine dysfunction, neutropenia, short stature, and skeletal abnormalities. In this report, we describe the case of a 14-year-old female with a history of neutropenia, pancreatic exocrine insufficiency and pancreatic endocrine sufficiency, pancreatic lipomatosis (10), and the development of myeloid leukemia. Postmortem examination revealed a high probability of SDS. We also describe the clinical findings in the patient's six siblings, suggesting this as a familial form of SDS. Because the gene(s) responsible for this syndrome have not yet been identified, genetic confirmation is not yet possible. This is the first report in the literature of a Mexican family with probable SDS.


Subject(s)
Abnormalities, Multiple/pathology , Bone and Bones/abnormalities , Cachexia/etiology , Isoamylase/deficiency , Pancreas/abnormalities , Trypsin/deficiency , Abnormalities, Multiple/genetics , Acute Disease , Adolescent , Bone Marrow/pathology , Calcinosis/etiology , Calcinosis/pathology , Celiac Disease/etiology , Child , Child, Preschool , Diarrhea/etiology , Dwarfism/etiology , Fatal Outcome , Female , Humans , Infant , Leukemia, Myeloid/etiology , Liver Cirrhosis/etiology , Male , Mexico , Neutropenia/genetics , Neutropenia/pathology , Nutrition Disorders/complications , Pancreas/pathology , Poverty , Shock, Septic/etiology , Syndrome
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