What is nemaline myopathy?
NEMALINE MYOPATHY
Alternate Name: Rod body disease
Age of Onset: Birth to adulthood
What is nemaline myopathy?
First described in 1963, nemaline myopathy is a disease of voluntary muscle
that is often nonprogressive. The most common form of the disease is not fatal,
although a rare form of the disorder is. Why is it called nemaline myopathy?
Nemaline means threadlike, and researchers chose this name because of the presence
in affected muscle cells of threadlike or rod-shaped material. The significance
of these rodlike bodies is still not clear.
What are the symptoms of nemaline myopathy?
People with nemaline myopathy have moderate weakness in their leg, arm and trunk
muscles, accompanied by some mild weakness of the face, tongue and throat muscles.
Reflexes are decreased or absent. Affected children often have long, narrow
faces with high-arched palates and slender body musculatures. High-arched feet
and curvature of the spine are common, and the jaw may also be malformed. The
severest form of nemaline myopathy usually appears at birth. Affected children
have a marked weakness and a lack of muscle tone. Their respiratory muscles
are weak, and death often occurs in the first few years of life due to respiratory
failure.
How are the muscle diseases known as inheritable myopathies inherited?
Most of these myopathies are inherited in an autosomal dominant pattern, which
means that a child need only inherit the defective gene from one parent in order
to have the disease. The parent transmitting the gene also has the disorder,
and each of his or her children has a 50 percent chance of inheriting the disease.
Autosomal refers to the fact that the genetic defect may be located on
any of the 46 rodlike structures, called chromosomes, that hold the genes found
in each human cell, except the two that determine a person's sex. With an autosomal
inheritance pattern, male and female children are equally affected. In rare
instances, some forms of these diseases appear to follow an autosomal recessive
pattern or an X-linked recessive pattern. A disease governed by the recessive
pattern requires that both parents, who usually do not have the disease, pass
on the defective gene in order for a child to be affected by the disease. Each
child of such parents has a 25 percent chance of inheriting and showing signs
of the disease. A 50 percent chance exists that such a child will inherit the
defective gene from only one parent and, therefore, will be a carrier of the
flawed gene and will usually not show signs of the disease. X-linked
refers to a gene that is on the X chromosome, which along with the Y chromosome
determines sex. Male children have one X chromosome and one Y chromosome, while
females have two X chromosomes. Therefore, inheritance
of a gene on the X chromosome is different from that for one on an autosomal
chromosome. In the X-linked recessive
pattern, the disease develops mostly in males. Females who inherit the defective
gene are usually carriers like their mothers
and can pass the disease on to their sons but rarely show signs of the disease
themselves. Central core disease, some forms
of myotonia congenita, myotubular myopathy (possibly), some forms of nemaline
myopathy, paramyotonia congenita and periodic paralysis follow the autosomal
dominant pattern. One form of myotonia congenita and some forms of nemaline
myopathy follow the autosomal recessive pattern. Some forms of myotubular myopathy
follow the X-linked recessive pattern.
Other Myopathies:
This is a group of un-related genetic muscle disorders, usually named for peculiarities
seen in biopsies of muscle tissue. Central core disease, usually apparent at
birth, causes skeletal deformities and diffuse weakness. Nemaline myopathy,
also usually apparent at birth, results in loss of muscle tone and progressive
weakness in limb and trunk muscles. Myotubular myopathy causes poor muscle tone
at birth and varying degrees of weakness in eye, facial, neck and limb muscles.
DOMINANT & RECESSIVE - The Simple Explanation
We all have two set of chromosomes (with all the various genes) - one set from
mom and the second set from dad. The sex chromosomes X and Y define our sex
- XX for girls, XY for boys. The rest of the chromosomes (# 1 to 22) are called
autosomes (hence where the term autosomal comes from). We each have two sets
of the autosomal chromosomes (# 1 to 22) which means that we also have TWO COPIES
of EACH GENE.
When a genetic condition is AUTOSOMAL DOMINANT, one of the genes is not working
right, and the gene that is "ok" cannot compensate for the affected
gene. Some types of NM are autosomal dominant.
With an autosomal dominant condition, the next generation has a 50% chance of
receiving the affected gene from the affected parent.
When a genetic condition is AUTOSOMAL RECESSIVE, both of the genes are not working
right. Other types of NM are autosomal recessive.
Children who show the recessive condition have inherited one affected gene from
mom and one affected gene from dad. Parents of the affected child are carriers
- they have one gene that is "ok", and the other gene is not working
right. In this case the "ok" gene can compensate for the affected
gene, and the carrier does not show signs of the condition. There is a 25% chance
of the next generation getting both affected genes from two carrier parents.
If the affected children then go on to have kids with a partner that has both
copies of the gene being "ok" - the next generation will be carriers
- get the affected gene from the affected parent and an "ok" gene
from the partner.
For families with more than one NM child and no prior history, autosomal recessive
is the given explanation. However, genetics is not always this straightforward
and there are more complex possibilities which will give a different outcome
in the subsequent generation - why more research needs to be done .......
By Daphne
(proud mother of two great kids, Taryn and Keelan, both with NM and no prior
family history of NM - note how we didn't follow the 25% genetic rule!)
Myopathy vs Dystrophy
A myopathy is any disease of the muscle (myo=muscle; pathos=disease). A dystrophy
is actually a class of myopathy that is characterized by progressive muscle
degeneration. Nemaline myopathy is known as a non- dystrophic myopathy because
muscle biopsies of patients with dystrophies look different under the microscope
and because NM is often non-progressive. It's easy to confuse the word myopathy
with dystrophy: both words refer to diseases that affect skeletal muscle, which
is the type of muscle that is responsible for movement and force.