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NARP syndrome

MONDO:0010794

A clinically heterogeneous progressive condition characterized by a combination of proximal neurogenic muscle weakness, sensory-motor neuropathy, ataxia, and pigmentary retinopathy.

Also known as: NARP syndrome, neurogenic muscle weakness-ataxia-retinitis pigmentosa syndrome, neuropathy-ataxia-retinitis pigmentosa syndrome, NARP, neuropathy ataxia retinitis pigmentosa syndrome, neuropathy, ataxia, and retinitis pigmentosa

19 clinical trials for this condition and its sub-types, 3 tagged with NARP syndrome itself.

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Part of

↑ Hereditary peripheral neuropathy (479) ↑ Mitochondrial oxidative phosphorylation disorder (58)

Including sub-types (19) Tagged with NARP syndrome (3)

Trials to join now! 2 Not yet finished but already full! 1

Massive gene hunt launched for mysterious mitochondrial diseases

Knowledge-focused By invitation only

This study aims to discover new genetic mutations that cause mitochondrial disorders by analyzing tissue samples from up to 6,900 participants. It includes people with suspected or known mitochondrial diseases, such as MELAS or Leigh's Disease, who lack a genetic diagnosis. The r…

Sponsor: Columbia University • Aim: Knowledge-focused

Last updated Jun 27, 2026 08:09 UTC

NARP syndrome

Where it sits in the disease tree

Massive gene hunt launched for mysterious mitochondrial diseases