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Summary
L-ARABINOSURIA
rare
autosomal dominant
symptoms
no consistent clinical signs or symptoms
onset, childhood
onset, infancy
laboratory finding
D-Arabitol mmol/mol creatinineurine
D-Arabitol +€mol/lplasma
Literature
Agrawal S,et al.Unusual case of failure to thrive: Type III Bartter syndromeJ Nepal Health Res Counc1434210-2132016