Orphanet: Renal caliceal diverticuli deafness syndrome
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Renal caliceal diverticuli-deafness syndrome

Disease definition

Renal caliceal diverticuli-deafness syndrome is a rare, syndromic, developmental defect during embryogenesis characterized by urinary tract and kidney anomalies, such as renal pelviocaliceal attenuation with multiple tiny caliceal diverticula, associated with sensorineural hearing loss. There have been no further descriptions in the literature since 1981.

ORPHA:2838

Classification level: Disorder
  • Synonym(s):
    • Renal caliceal diverticuli-hearing loss syndrome
  • Prevalence: <1 / 1 000 000
  • Inheritance: -
  • Age of onset: Neonatal
  • ICD-10: Q64.8
  • OMIM: -
  • UMLS: -
  • MeSH: -
  • GARD: 4655
  • MedDRA: -

  A summary on this disease is available in Español (2018) Italiano (2018) Nederlands (2018) Polski ()

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The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.