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      • Signs and symptoms are typically present at birth and include hypotonia, muscle weakness, developmental delay, intellectual disability and occasional seizures. It is also associated with lissencephaly, hydrocephalus, cerebellar malformations, eye abnormalities, and other abnormalities.
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  2. Aug 17, 2022 · What are the symptoms of Walker-Warburg syndrome? Walker-Warburg syndrome causes symptoms that affect your child’s muscles, brain and eyes. Symptoms range in severity and are usually present at birth or early infancy. Symptoms can be life-threatening. Muscle symptoms

  3. Apr 1, 2022 · Signs & Symptoms. The main symptoms of WWS are muscular dystrophy (progressive degeneration and weakness of the voluntary muscles) and abnormalities of the brain and eyes. Symptoms of WWS are congenital (present at birth), and some of the brain abnormalities can be detected by prenatal ultrasound and/or fetal MRI in the later stages of pregnancy.

  4. Walker-Warburg syndrome (WWS) is a severe form of congenital muscular dystrophy associated with brain and eye abnormalities. Signs and symptoms are typically present at birth and include hypotonia, muscle weakness, developmental delay, intellectual disability and occasional seizures.

  5. It is the most severe of a group of genetic conditions known as congenital muscular dystrophies, which cause muscle weakness and wasting (atrophy) beginning very early in life. The signs and symptoms of Walker-Warburg syndrome are present at birth or in early infancy.

  6. What are the typical symptoms of Walker-Warburg Syndrome? Typical symptoms of Walker-Warburg Syndrome (WWS) include muscle weakness, poor muscle tone, respiratory problems, seizures, and vision and hearing impairments.

  7. Walker-Warburg syndrome (WWS) is a very rare and severe congenital muscular dystrophy that affects the brain, eyes and muscles. WWS belongs to a group of conditions known as dystroglycanopathies. Signs and symptoms of the condition are typically present before birth or very shortly afterward.

  8. Walker-Warburg syndrome (WWS) is a severe form of congenital muscular dystrophy associated with brain and eye abnormalities. Signs and symptoms are typically present at birth and include hypotonia, muscle weakness, developmental delay, intellectual disability and occasional seizures.

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