Non-Type I Cystinuria Associated with Mental retardation and Ataxia in a Korean Boy with a New Missence Mutation(G173R) in the SLC7A9 Gene.
10.3346/jkms.2010.25.1.172
- Author:
Eun Ha LEE
1
;
Yeun Hee KIM
;
Jin Soon HWANG
;
Sung Hwan KIM
Author Information
1. Department of Pediatrics and Research Laboratory for Mitochondrial Disorders, Ajou University School of Medicine, Suwon, Korea. pedkim@ajou.ac.kr
- Publication Type:Case Reports ; Research Support, Non-U.S. Gov't
- Keywords:
Non-type I Cystinuria;
Neurologic Manifestations;
SLC7A9;
Mutation
- MeSH:
Adolescent;
Amino Acid Substitution;
Amino Acid Transport Systems, Basic/*genetics;
Amino Acids/urine;
Ataxia/complications/diagnosis/*genetics;
Base Sequence;
Cystine/blood;
Cystinuria/complications/diagnosis/*genetics;
Humans;
Intellectual Disability/complications/diagnosis/*genetics;
Male;
*Mutation, Missense;
Pedigree;
Republic of Korea
- From:Journal of Korean Medical Science
2010;25(1):172-175
- CountryRepublic of Korea
- Language:English
-
Abstract:
Cystinuria is an inherited renal and intestinal disease characterized by defective amino acids reabsorption and cystine urolithiasis. It is unusually associated with neurologic symptoms. Mutations in two genes, SLC3A1 and SLC7A9, have been identified in cystinuric patients. This report presents a 13-yr-old boy with cystinuria who manifested difficulty in walking, ataxia, and mental retardation. Somatosensory evoked potential of posterior tibial nerve stimulation showed the central conduction dysfunction through the posterior column of spinal cord. He was diagnosed non-type I cystinuria by urinary amino acid analysis and oral cystine loading test. We screened him and his family for gene mutation by direct sequencing of SLC3A1 and SLC7A9 genes. In this patient, we identified new missence mutation G173R in SLC7A9 gene.
