All individuals with variants in gene TPI1

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00408101 194 PubMed: Alabdullatif 2017 - F yes United Arab Emirates - - - - - retinal disease 2 years old girl was born with uncomplicated antenatal course. During the neonatal period she developed persistent jaundice that required phototherapy and hemolytic anemia that required blood transfusions. During infancy, she continued to have macrocytic hemolytic anemia and found to have esotropia, failure to thrive, short stature, regression, hypotonia, hypereflexia, and joint hyperlaxity. Parents were cousins. She had two healthy siblings. 1 1 LOVD
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