Document Detail


Neonatal intrahepatic cholestasis caused by citrin deficiency in two Malaysian siblings: outcome at one year of life.
MedLine Citation:
PMID:  20200759     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
We report two Malaysian siblings with neonatal intrahepatic cholestasis caused by citrin deficiency (NICCD). The younger sibling, a six-month-old Chinese girl, presented with prolonged neonatal jaundice, and was investigated for biliary atresia. Urine metabolic screen showed the presence of urinary-reducing sugars, and she was treated with a lactose-free formula. NICCD was suspected based on the clinical history, examination and presence of urinary citrulline. Mutation study of the SLC25A13 gene showed the compound heterozygotes, 851del4 and IVS16ins3kb, which confirmed the diagnosis of NICCD in the patient and her three-year-old female sibling, who also had unexplained neonatal cholestasis. Long-term dietary advice, medical surveillance and genetic counselling were provided to the family. The diagnosis of NICCD should be considered in infants with unexplained prolonged jaundice. DNA-based genetic testing of the SLC25A13 gene may be performed to confirm the diagnosis retrospectively. An awareness of this condition may help in early diagnosis using appropriate metabolic and biochemical investigations, thus avoiding invasive investigations in infants with neonatal cholestasis caused by NICCD.
Authors:
M K Thong; C C Boey; J S Sheng; M Ushikai; K Kobayashi
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Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  Singapore medical journal     Volume:  51     ISSN:  0037-5675     ISO Abbreviation:  Singapore Med J     Publication Date:  2010 Jan 
Date Detail:
Created Date:  2010-03-04     Completed Date:  2010-07-08     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  0404516     Medline TA:  Singapore Med J     Country:  Singapore    
Other Details:
Languages:  eng     Pagination:  e12-4     Citation Subset:  IM    
Affiliation:
Genetics and Metabolism Unit, Department of Paediatrics, Faculty of Medicine, University of Malaya, Kuala Lumpur 50603, Malaysia. thongmk@um.edu.my
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MeSH Terms
Descriptor/Qualifier:
Calcium-Binding Proteins / deficiency*
Child, Preschool
Cholestasis, Intrahepatic / etiology,  genetics*,  therapy
Diet Therapy
Female
Gene Deletion
Genetic Counseling
Humans
Infant
Malaysia
Metabolism, Inborn Errors / diagnosis,  genetics*
Mitochondrial Membrane Transport Proteins / genetics*
Organic Anion Transporters / deficiency*
Siblings
Chemical
Reg. No./Substance:
0/Calcium-Binding Proteins; 0/Mitochondrial Membrane Transport Proteins; 0/Organic Anion Transporters; 0/SLC25A13 protein, human; 1340-08-5/citrin

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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