A novel mutation in a large family causes a unique phenotype of Mucolipidosis IV

作者：AlBakheet AlBandary; Qari Aliya; Colak Dilek; Rasheed Anas; Kaya Namik^*; Al Sayed Moeenaldeen

来源：Gene, 2013, 526(2): 464-466.

DOI：10.1016/j.gene.2013.04.076

• MCOLN1
• Novel p.Y436C
• ML IV
• Gastrin

Mucolipidosis type IV is a rare autosomal recessive lysosomal storage disorder reported among Ashkenazi Jews and to a lesser extent in other ethnic groups. Several mutations have been reported in MCOLN1 which is the only known gene associated with the disorder. Here we report the first Saudi patient with Mucolipidosis type IV from a consanguineous family with two branches having a total of five patients carrying a novel transition mutation, c.1307A > G (p.Y436C) in exon 11. The clinical course of the patient was nonspecific and a lysosomal storage disorder was not highly suspected due to lack of coarse facial features, organomegaly and skeletal findings of dysostosis multiplex. The detailed bioinformatics analysis on the deleterious effects of the mutation is discussed. Emphasis is made on the importance of brain magnetic resonance imaging (MRI) findings and serum gastrin level as key clues to the diagnosis of this often subtle neurodevelopmental disorder.

• 出版日期2013-9-10