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Hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome
Disease definition
Hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome is a rare, genetic, mitochondrial disease characterized by early-onset progressive renal failure, manifesting with hyperuricemia, hyponatremia, hypomagnesemia, hypochloremic metabolic alkalosis, elevated BUN and polyuria, associated with systemic manifestations which include pulmonary hypertension, failure to thrive, global developmental delay, hypotonia and ventricular hypertrophy. Additional features include prematurity, elevated serum lactate, diabetes mellitus and, in some, pancytopenia.
ORPHA:363694
Classification level: Disorder- Synonym(s):
- HUPRA syndrome
- Prevalence: <1 / 1 000 000
- Inheritance: Autosomal recessive
- Age of onset: Infancy, Neonatal
- ICD-10: N15.8
- OMIM: 613845
- UMLS: -
- MeSH: -
- GARD: -
- MedDRA: -
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