Papillorenal syndrome differential diagnosis: Difference between revisions

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* Branchio-oto-renal syndrome- Renal hypoplasia in these patients makes this an important differential.
* Branchio-oto-renal syndrome- Renal hypoplasia in these patients makes this an important differential.


* Pt with PAX6 Mutations - significant overlap with eye findings in patients with PAX6 gene mutation make it an important differential but the renal anomalies are usually absent in these patients.  
* Pt with PAX6 Mutations - significant overlap with eye findings in patients with PAX6 gene mutation make it an important differential but the renal anomalies that are typical for RCS are absent in these patients.  


* COACH Syndrome or Joubert - Important differential due to the presence of both renal abnormalities and colobomas in these patients. However, patients with Renal coloboma syndrome does not have any developmental abnormality, cerebellar abnormalities, and/or hepatic dysfunction.
* COACH Syndrome or Joubert - Important differential due to the presence of both renal abnormalities and colobomas in these patients. However, patients with Renal coloboma syndrome does not have any developmental abnormality, cerebellar abnormalities, and/or hepatic dysfunction.

Revision as of 18:55, 5 September 2020

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Various differential diagnosis of renal coloboma syndrome are as follows:

  • CHARGE syndrome
    • Coloboma
    • Heart Abnormalities
    • Choanal Atresia
    • Growth and development Retardation
    • Genital Anomalies
    • Ear and hearing abnormalities

A lot of patients studied under renal coloboma syndrome do not have any sort of craniofacial anomalies that are typical of CHARGE Syndrome.

  • Branchio-oto-renal syndrome- Renal hypoplasia in these patients makes this an important differential.
  • Pt with PAX6 Mutations - significant overlap with eye findings in patients with PAX6 gene mutation make it an important differential but the renal anomalies that are typical for RCS are absent in these patients.
  • COACH Syndrome or Joubert - Important differential due to the presence of both renal abnormalities and colobomas in these patients. However, patients with Renal coloboma syndrome does not have any developmental abnormality, cerebellar abnormalities, and/or hepatic dysfunction.
  • Cat Eye Syndrome - This genetic abnormality is having symptomatic overlap with renal coloboma syndrome but the Iris colobomas that are typical for RCS are usually not observed in this disorder.

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