Amyotonia congenita

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Used for

benign congenital hypotonia, congenital myopathy benign, floppy amyotonic infant

Broader Terms

congenital neuromuscular disorder, spinal cord disorder

Facts (generated by robot; please edit if you find it inaccurate)

  • Doctors said I had amyotonia congenita and predicted I wouldnt live past my 8th birthday.
  • Amyotonia congenita1 is a congenital, sometimes familial, disorder, characterised by muscular hypotonia and hypoplasia without atrophy.
  • 44 Human Disease and Mouse Model Detail Human Disease Term: Amyotonia Congenita OMIM ID: 205000 Synonyms Oppenheim Disease Associated Genes There are currently no human or mouse genes associated with this disease in the MGI database.
  • PDF THE PATHOLOGICAL EXAMINATION OF TWO CASES OF AMYOTONIA CONGENITA WITH THE CLINICAL.
  • PDF ON AMYOTONIA CONGENITA TURNER Brain.

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