Phenotypes for disease #00057 (MSUD1A (maple syrup urine disease, type Ia), OMIM:248600)

9 entries on 1 page. Showing entries 1 - 9.
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Diagnosis/Definite     

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Age/Examination     

Age/Onset     

Phenotype/Onset     

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Individual ID     
0000000025 - - - Isolated (sporadic) - - - - - Alfonso Luis Oyarzábal Sanz 00000207
0000143241 (HPO:0010910) Hypervalinemia (HPO:0010911) Hyperleucinemia (HPO:0010913) Hyperisoleucinemia - - Familial, autosomal recessive - - - - - Belen Perez 00180974
0000143310 - - - Familial, autosomal recessive - - - - - Belen Perez 00181057
0000235174 see paper; ... maple syrup urine disease, type 1A MSUD Unknown - - - - - Johan den Dunnen 00309859
0000337124 progressive encephalopathy since day 5 after birth with poor suckling, vomiting, irritability and consequently lethargy so admitted in NICU when he was 8 days old. He developed convulsions with respiratory distress therefore, underwent mechanically ventilation and antibiotic regimen for presumptive neonatal sepsis but without improvement. Initial biochemical investigations showed metabolic acidosis and a mild elevated ammonia. Further biochemical analysis of expanded metabolic screening of amino acids and acylcarnitines at 18 days of age revealed marked elevated BCAAs in blood and nonspecific elevation of 4-OH phenyl lactate and 4-OH phenyl pyruvate on urine organic acid analysis by GC-MS marked elevation of leucine/isoleucine 3590µmol/l and also show significant elevation on several occasions of metabolic stress MUSD Familial, autosomal recessive 00y00m08d 00y00m05d - 00y00m18d - Zeinab Sayed Abdelkhalek 00446898
0000339382 Microcephaly, intellectual disability, inappropriate laughter, optic nerve atrophy, atrial septal defect, congenital hip dysplasia Maple syrup urine disease Maple syrup urine disease, type Ib Familial, autosomal recessive 00y01m - - 00y01m - Miriam Erandi Reyna-Fabián 00450321
0000340292 - Maple syrup urine disease Maple syrup urine disease, type Ia Familial, autosomal recessive - - - 00y01m - Miriam Erandi Reyna-Fabián 00451630
0000340298 Global developmental delay, Spasticity, Amblyopia Maple syrup urine disease Maple syrup urine disease, type II Familial, autosomal recessive - - 03y06m 00y03m - Miriam Erandi Reyna-Fabián 00451637
0000340323 Global developmental delay Maple syrup urine disease MSUD1A: Maple syrup urine disease, type II Familial, autosomal recessive - - - 00y03m - Miriam Erandi Reyna-Fabián 00451662
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