Anonychia congenita
A genetic congenital neuromuscular disorder affecting the skeletal muscles. It is caused by mutations in the chloride channel gene (CLCN1 gene). It is characterized by muscle stiffness, hypertrophy, pain, and cramping.
Disease Alternative Name
myotonia congenita
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Recent Cases of Anonychia congenita
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Top doctors who continously share their opinions on Anonychia congenitaBaramati
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METPALLY KARIMNAGAR
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MANIKRISHNA MS HOSPITAL
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British Paediatric Neurology Association
NeoNate Neurology

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Barpali
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Self Employed. Now Doing My Practice
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Worked at Jalna.Latur. and Now Mumbai.
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Consulting Surgeon.
M.S.,FICS,FAIS. Sr. Surgeon.

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