PURPOSE: To assess for KIF21A mutation in the first two reported Saudi Arabian families with the classic phenotype of congenital fibrosis of the extraocular muscles type I (CFEOM1). METHODS: Clinical examination and genetic testing by amplification refractory mutation system (ARMS) assay for KIF21A R954W, the most common KIF21A mutation worldwide. RESULTS: Clinical examination was consistent with classic CFEOM1 in both Family A and Family B. All participating patients (one child from Family A and four adults from Family B) were heterozygous for KIF21A R954W mutation. CONCLUSIONS: CFEOM1 is rare is Saudi Arabia as it is in the rest of the world. The finding of R954W mutation in the historically isolated population of the Arabian Peninsula confirms that R954 is a "hotspot" for KIF21A mutation.
PURPOSE: To assess for KIF21A mutation in the first two reported Saudi Arabian families with the classic phenotype of congenital fibrosis of the extraocular muscles type I (CFEOM1). METHODS: Clinical examination and genetic testing by amplification refractory mutation system (ARMS) assay for KIF21AR954W, the most common KIF21A mutation worldwide. RESULTS: Clinical examination was consistent with classic CFEOM1 in both Family A and Family B. All participating patients (one child from Family A and four adults from Family B) were heterozygous for KIF21AR954W mutation. CONCLUSIONS:CFEOM1 is rare is Saudi Arabia as it is in the rest of the world. The finding of R954W mutation in the historically isolated population of the Arabian Peninsula confirms that R954 is a "hotspot" for KIF21A mutation.
Authors: Arif O Khan; Jameela Shinwari; Aisha Omar; Latifa Al-Sharif; Dania S Khalil; Mohammed Alanazi; Abdullah Al-Amri; Nada Al Tassan Journal: Mol Vis Date: 2011-01-20 Impact factor: 2.367