An extremely rare subtype of hereditary motor and sensory neuropathy with characteristics of severe, rapidly progressing, distal, symmetric polyneuropathy and microcephaly (which can be evident in utero) with intact cognition. Clinically it presents
syndrome de microcephalie-neuropathie sensitivo-motrice axonale complexe
SNOMEDCT-BE (which can be evident in utero) with intact cognition. Clinically it presents / 763798008
SNOMEDCT-BE (disorder) / 763798008