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Alkaptonuria, a new association of distal renal tubular acidosis
Author(s) -
Azar Nickavar,
Maryam Razzaghy Azar
Publication year - 2018
Publication title -
saudi journal of kidney diseases and transplantation/našrat amraḍ wa zira'aẗ al-kulaẗ
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.268
H-Index - 30
eISSN - 2320-3838
pISSN - 1319-2442
DOI - 10.4103/1319-2442.239645
Subject(s) - alkaptonuria , medicine , renal tubular acidosis , distal renal tubular acidosis , tubulopathy , complication , acidosis , connective tissue disorder , pathology , endocrinology , kidney , dermatology
Alkaptonuria (ALK) is a rare genetic disorder, characterized by binding of ochronotic pigment to the connective tissues in different tissues. This is the first report of a child presented with primary distal renal tubular acidosis associated with ALK. Both disorders were managed by their specific medical treatments, with no further complication.

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