asked 226k views
3 votes
Werdnig-Hoffmann disease is the infantile form (type 1) of Spinal muscular atrophy (SMA).

1) True
2) False

asked
User Tnilsson
by
8.5k points

1 Answer

4 votes

Final answer:

Werdnig-Hoffmann disease is the infantile form of Spinal muscular atrophy (SMA).

Step-by-step explanation:

The statement is True. Werdnig-Hoffmann disease is indeed the infantile form (type 1) of Spinal muscular atrophy (SMA). SMA is a genetic disorder that affects the control of muscle movement. It is characterized by the degeneration of motor neurons in the spinal cord, leading to muscle weakness and atrophy.

answered
User Couto
by
7.5k points
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