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Brain Dev. 2014 Mar;36(3):264-7. doi: 10.1016/j.braindev.2013.03.005. Epub 2013 Apr 20.

Prenatal diagnosis of citrullinemia type 1: a Chinese family with a novel mutation of the ASS1 gene.

Author information

1
Department of Pediatrics, Peking University First Hospital, Beijing 100034, China.
2
Department of Pediatrics, Peking University First Hospital, Beijing 100034, China. Electronic address: yanlingy@vip.sina.com.

Abstract

BACKGROUND:

Argininosuccinate synthetase deficiency (citrullinemia type 1) is a rare autosomal recessive disorder of the urea cycle characterized by elevated concentrations of citrulline, ammonia, and orotic acid, manifesting with acute hyperammonemic crises, usually early in life, with concurrent neurologic deterioration. Only a few cases of citrullinemia type 1 have been documented from mainland China. Prenatal diagnosis has not been performed.

METHODS:

A Chinese family affected by citrullinemia type 1 was studied. The proband, a girl, was the second child born to a non-consanguineous couple. Her elder brother died at 19months due to coma and liver dysfunction of unknown cause. The proband was admitted because of severe mental retardation and lethargy at the age of 15months. Initial laboratory results revealed hyperammonaemia, hypercitrullinemia (928.771μmol/L, normal 5.0-25.0μmol/L) and orotic aciduria, supporting the diagnosis of citrullinemia type 1. Subsequently, the mother presented at 15weeks of pregnancy seeking for genetic counseling and prenatal diagnosis. ASS1 gene in the blood leukocytes of the family members and amniocytes was performed by direct sequencing.

RESULTS:

On the ASS1 gene of the proband, a novel mutation, T1009C (C337R), and a previously reported mutation G847A (E283K) were identified. Each parent carries one of two mutations. G847A and T1009C mutations were detected in amniocytes, as same as the proband of the family. The result revealed that the fetus was affected by argininosuccinate synthetase deficiency. The parents chose to have a termination of the pregnancy.

CONCLUSIONS:

Prenatal diagnosis for citrullinemia type 1 was performed in a Chinese family using gene analysis. T1009C (C337R), a novel mutation of ASS1, was identified.

KEYWORDS:

ASS1 gene; Argininosuccinate synthetase; Citrullinemia type 1; Prenatal diagnosis

PMID:
23611581
DOI:
10.1016/j.braindev.2013.03.005
[Indexed for MEDLINE]
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