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Werdnig-Hoffmann disease is the infantile form (type 1) of Spinal muscular atrophy (SMA).

1) True
2) False

User Tnilsson
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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.

User Couto
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