A 53-year-old man noticed difficulty relaxing his hand grip after a hand shake at age 35. Gradually he developed stiffness of the legs muscles and cataract. His asymptomatic daughter's examination revealed grip and percussion myotonia. Watch the video at PracticalNeurology.net. Direct link: http://bmctoday.net/practicalneurology/videos.asp?f=video6
The earlier appearance of symptoms in the daughter is due to a phenomenon called:
- Variable Penetrance
Find the answer and diagnosis in the next edition of Practical Neurology or online, posted along with the patient video at PracticalNeurology.net
Case selected from Dr. Shaibani's Video Atlas of Neuromuscular Diseases, in press, by Oxford University Press. Aziz Shaibani, MD, FACP, FAAN is Director of Nerve & Muscle Center of Texas and Clinical Associate Professor of Medicine at Baylor College of Medicine in Houston, TX. He is also Adjunct Professor of Neurology at Kansas University Medical Center in Kansas City, Kansas.
Diagnosis: Kennedy Disease
Last month's case presented a 42-year-old man who showed atrophy and fasciculations of the tongue, abnormal facial movements, and large breasts.
BY AZIZ SHAIBANI, MD
Read the case description and watch the video online at PracticalNeurology.net.
Mutation of which of the following genes is expected in this case?
- Androgen receptors(AR)
- Superoxide dismutase(SOD)
- Valosin containing protein (VCR)
- TAR DNA-binding protein 43 (TDP-43)
- FUS (Fused in Sarcoma)
Diagnosis: Kennedy disease (X-linked bulbospinal muscular atrophy)
It is an X-linked recessive disease caused by a mutation of the androgen receptor gene on Xq12. The mutation is in the form of CAG repeat expansion.
- Most affected people have a repeat number of 40-65 (normal range is 10-36).
- CTG repeats produce Polyglutamine tail, which leads to abnormal folding of the androgen receptors resulting in partial proteolysis. Androgen plasy a role in cells survival and dendritic growth.
- Autosomal dominant bulbospinal atrophy with gynecomastia is also reported.
Pathologically, the disease is characterized by degenration of the motor and sensory neurons. Extraocular muscles are spared, may be due to low number of androgen receptors.
Anticipation (earlier onset and more severe disease in subsequent generations) has not ben substantiated.
Age of onset: 15-60 years.
Heterozygous female may display tongue fasciculations and muscle cramps int he 7th decade.
Musce cramps, fatigue, and legs weakness are common early symtpoms.
Full blown picture:
- Proximal weakness, atrophy and fascicluations.
- Tongue weakness and fasciulations.
- Facial myokymia.
- Dysphagia, dysarthria.
- Diffuse areflexia.
- Reduced feet sensation and small sensory nerve action potentials(SNAPS). Action tremor.
- Gynecomastia, testicular atrophy, erectile dysfunction.
- Diabetes Mellitus.
- Needle electromyography: chronic diffuse denervation.
Mildly elevated creatine Kinase(CK).
It affects 2:100,000 of population.
Every male with muscle cramps, high CK and neurogenic EMG should be tested for Kennedy disease.
In chronic motor neuron disorders, the presence of high CK and low SNAPS whould raise the posibility of Kennedy's syndrome
Due to rarity and protean manefestations, Kennedy disease may be misdiagnosed as:
- Myopathy: due the presence of proximal symmetrical weakness,
- Muscle cramps, and elevated CK.
- Neuropathy: due to the presence of feet numbness, areflexia, and low SNAPS.
- Myasthenia gravis: due to the presence of dysphagia, dysarthria, fatigability of chewing muscles and jaw ptosis (due to trigeninal neuropathy).
- ALS: due to the presence of tongue fasciculations and wide spread denervation.
The disease is slowly progressive and is not curable.