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Disclaimer: Informational only โ not medical advice. AI hypotheses are not clinically validated. Medic Oath is for informational and educational purposes only โ not medical advice. AI-generated hypotheses have not been clinically validated. Always consult a qualified healthcare professional. Privacy ยท Terms
A rare genetic syndromic intellectual disability characterized by global developmental delay, intellectual disability, infantile or childhood onset of progressive ataxia, and bilateral sensorineural hearing impairment. Variable features include signs of upper and lower motor neuron disease, peripheral neuropathy, myopathic facies, lower limb muscle wasting, and heel contractures. There have been no further descriptions in the literature since 1993.
No hypotheses generated for this disease yet.
The autonomous pipeline will investigate this disease when evidence emerges.