Contents
- 1 Waddling gait also known as -
- 2 Waddling gait seen in all of the following EXCEPT -
- 3 Scissors gait seen in -
- 4 Steppage gait seen in -
- 5 HTT gene is located on the short arm (p) of chromosome ----------
- 6 Motor symptoms of Parkinsonism result from the death of cells in -
- 7 Wilson's disease gene (ATP7B) is on chromosome number ------
- 8 Which disease is the most common from a group of hereditary diseases that cause copper overload in the liver?
- 9 Lactic acidosis is seen in deficiency of -
- 10 Overexpression of superoxide dismutase-1[SOD1]has been linked to the neural disorders seen in -
Waddling gait also known as -
Myopathic gait also known as waddling gait is a form of gait abnormality.
The "waddling" is due to the weakness of the proximal muscles of the pelvic girdle
Waddling gait seen in all of the following EXCEPT -
Conditions associated with a myopathic gait -
pregnancy,
congenital hip dysplasia,
muscular dystrophies,
spinal muscular atrophy
Scissors gait seen in -
Knees and thighs hit or cross in a scissors-like pattern when walking
The steps are slow and small. This type of gait occurs often in patients with spastic cerebral palsy.
Steppage gait seen in -
“high stepping” type of gait in which the leg is lifted high, the foot drops, appearing floppy, and the toes points downward, scraping the ground, when walking.
HTT gene is located on the short arm (p) of chromosome ----------
Huntington's disease is a progressive brain disorder caused by a single defective gene on chromosome 4
Mutated HTT is the cause of Huntington's disease
Motor symptoms of Parkinsonism result from the death of cells in -
Parkinsonism - motor symptoms of the disease result from the death of cells in the substantia nigra
Wilson's disease gene (ATP7B) is on chromosome number ------
Wilson's disease - inherited in an autosomal recessive pattern
Wilson's disease gene (ATP7B) is on chromosome 13
Which disease is the most common from a group of hereditary diseases that cause copper overload in the liver?
Wilson's disease is the most common from a group of hereditary diseases that cause copper overload in the liver.
All can cause cirrhosis at a young age
Lactic acidosis is seen in deficiency of -
Pyruvate carboxylase deficiency - Lactic acidosis and Hyperammonaemia
Overexpression of superoxide dismutase-1[SOD1]has been linked to the neural disorders seen in -
SOD1 is located in the cytoplasm, SOD2 in the mitochondria, and SOD3 is extracellular.
Overexpression of SOD1 has been linked to the neural disorders seen in Down syndrome
