The article describes the clinical signs (symptoms) of a rare storage disease in eleven Yakut infants. All the children were from unrelated families. The disease is very severe, leading to the disability and death at an early age. Diagnostics using the most complicated and advanced biochemical methods hasn't produced results.
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Sheikh Khalifa Med City, Dept Ophthalmol, Abu Dhabi, U Arab Emirates
Princess Alexandra Eye Pavil, Dept Ophthalmol, Edinburgh, Midlothian, ScotlandSheikh Khalifa Med City, Dept Ophthalmol, Abu Dhabi, U Arab Emirates
Chan, Tin K.
Alkaabi, Mohammed K.
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Sheikh Khalifa Med City, Dept Ophthalmol, Abu Dhabi, U Arab EmiratesSheikh Khalifa Med City, Dept Ophthalmol, Abu Dhabi, U Arab Emirates
Alkaabi, Mohammed K.
ElBarky, Ahmed M.
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Sheikh Khalifa Med City, Dept Ophthalmol, Abu Dhabi, U Arab Emirates
Benha Univ, Benha Fac Med, Banha, EgyptSheikh Khalifa Med City, Dept Ophthalmol, Abu Dhabi, U Arab Emirates
ElBarky, Ahmed M.
El-Hattab, Ayman W.
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Tawam Hosp, Div Genet & Metab Disorders, Al Ain, U Arab EmiratesSheikh Khalifa Med City, Dept Ophthalmol, Abu Dhabi, U Arab Emirates
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King Faisal Specialist Hosp & Res Ctr, Dept Genet, Riyadh 11211, Saudi ArabiaKing Faisal Specialist Hosp & Res Ctr, Dept Genet, Riyadh 11211, Saudi Arabia
Anazi, S.
Al-Sabban, E.
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King Faisal Specialist Hosp & Res Ctr, Div Nephrol, Dept Pediat, Riyadh 11211, Saudi ArabiaKing Faisal Specialist Hosp & Res Ctr, Dept Genet, Riyadh 11211, Saudi Arabia
Al-Sabban, E.
Alkuraya, F. S.
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King Faisal Specialist Hosp & Res Ctr, Dept Genet, Riyadh 11211, Saudi Arabia
Alfaisal Univ, Coll Med, Dept Anat & Cell Biol, Riyadh, Saudi ArabiaKing Faisal Specialist Hosp & Res Ctr, Dept Genet, Riyadh 11211, Saudi Arabia