Nemaline Myopathy (NM) is a genetic muscle disorder that affects approximately one in 50,000 people, often showing symptoms from birth. Its name comes from the presence of “nemaline bodies ...

What is Nemaline Myopathy? Nemaline myopathy is a congenital, often hereditary, neuromuscular disorder that primarily affects skeletal muscles, which are responsible for voluntary movements.

Nemaline myopathy, or rod myopathy, is a rare congenital disease affecting skeletal muscles, causing muscle weakness. The condition is hereditary and caused by genetic mutations affecting muscle ...

A new comprehensive natural history study about Amish nemaline myopathy (ANM) in the Old Order Amish population focuses on the promise of gene therapy for this lethal disorder. Amish nemaline ...

How 25-year-old Linges Warry Apparao, who has a rare disease known as nemaline rod myopathy, learnt to embrace her uniqueness.

We learned about a year ago that Melaina has a disease called Nemaline Rod Myopathy. It causes severe muscle weakness and is usually fatal among infants. One reason we feel very fortunate today ...

CJI DY Chandrachud addressed the lack of awareness regarding nemaline myopathy among doctors and parents during a national consultation on children's rights.

Caused by a gene mutation, nemaline rod myopathy has an estimated incidence of 1 in 50,000 individuals, according to the U.S. National Library of Medicine. While there are variations that impact ...

A new comprehensive natural history study about Amish nemaline myopathy (ANM) in the Old Order Amish population focuses on the promise of gene therapy for this lethal disorder. Amish nemaline ...