SciELO - Scientific Electronic Library Online

 
vol.19 issue1Simplified method of CPAP titration in patients with diagnosis of Obstructive Sleep Apnea: Case series using the autoadjustable Autoset T author indexsubject indexarticles search
Home Pagealphabetic serial listing  

Services on Demand

Journal

Article

Indicators

  • Have no cited articlesCited by SciELO

Related links

  • Have no similar articlesSimilars in SciELO

Share


Revista Medica Herediana

Print version ISSN 1018-130XOn-line version ISSN 1729-214X

Abstract

TAPIA ZERPA, Carlos Enrique  and  MIYAHIRA ARAKAKI, Juan. Autosomal recessive Alport syndrome: A case report. Rev Med Hered [online]. 2008, vol.19, n.1, pp.25-28. ISSN 1018-130X.

Woman, 14 year old from San Martin (Peru), was admitted to hospital with a history of three months of dyspnea, pallor and hyporexia, and decreased urine volume in the last month. Two weeks before his admission presented overall headache, nausea and vomiting. She went to his local hospital where indicated treatment with ampicillin and gentamicin, on suspicion of acute pyelonephritis; but not observe improvement was transferred to our hospital. There were no important personal or family history, except her parents were consanguineous. On physical examination we found pallor, bilateral opacities in the lens, bilateral hearing loss and flapping. Laboratory tests showed anemia and azotemia (creatinine 15 mg/dL and urea 233 mg/dL). Urianalysis revealed tubular abnormalities, proteinuria and hematuria. Renal ultrasonography showed small kidneys. Ocular examination revealed nuclear polar cataract in her right eye and total cataract in the left eye. Audiometry revealed bilateral sensorineural hearing loss. (Rev Med Hered 2008;19:25-28).

Keywords : Alport; hematuria; hypoacusia; renal failure.

        · abstract in Spanish     · text in Spanish     · Spanish ( pdf )