An unusual renal complication in a patient with osteogenesis imperfecta

Lavjay Butani, Julia A. Rosekrans, Bruce Z. Morgenstern, Dawn S. Milliner

Research output: Contribution to journalArticle

7 Citations (Scopus)

Abstract

Osteogenesis imperfecta (OI) is a common 'rare' disorder with a reported incidence of 1/15,000 to 1/20,000 in newborns. Skeletal abnormalities in this condition are so striking that its equally important and diverse extraskeletal manifestations frequently remain unnoticed. Sensorineural deafness, blue sclerae, myopia, easy bruisability, dental anomalies, and floppy mitral valves are some of its more frequently reported extraskeletal features. Other less common features include pulmonary hypoplasia, joint contractures, hydrocephalus, and osteogenic sarcoma.1-3. Our patient, a 16-year-old boy, developed a previously unreported complication: chronic renal failure, which on subsequent evaluation was attributed to obstructive uropathy secondary to bony pelvic outlet deformities.

Original languageEnglish (US)
Pages (from-to)489-491
Number of pages3
JournalAmerican Journal of Kidney Diseases
Volume25
Issue number3
DOIs
StatePublished - 1995
Externally publishedYes

Fingerprint

Osteogenesis Imperfecta
Mitral Valve Prolapse
Sclera
Myopia
Contracture
Deafness
Hydrocephalus
Chronic Kidney Failure
Tooth
Joints
Newborn Infant
Kidney
Lung
Incidence

Keywords

  • chronic renal failure
  • Osteogenesis imperfecta
  • pelvic outlet obstruction
  • protrusio acetabuli

ASJC Scopus subject areas

  • Nephrology

Cite this

An unusual renal complication in a patient with osteogenesis imperfecta. / Butani, Lavjay; Rosekrans, Julia A.; Morgenstern, Bruce Z.; Milliner, Dawn S.

In: American Journal of Kidney Diseases, Vol. 25, No. 3, 1995, p. 489-491.

Research output: Contribution to journalArticle

Butani, Lavjay ; Rosekrans, Julia A. ; Morgenstern, Bruce Z. ; Milliner, Dawn S. / An unusual renal complication in a patient with osteogenesis imperfecta. In: American Journal of Kidney Diseases. 1995 ; Vol. 25, No. 3. pp. 489-491.
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