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The following Conditions are related to Weakening and loss of muscle at birth

Select a specific condition below to view its details.

  • Hard syndrome

    Congenital muscular dystrophy in its most severe form, hard +/-e syndrome, is accompanied by abnormalities of the brain and eyes. Typical signs and symptoms include hypotonia, muscle weakness, developmental delay, intellectual dysfunction, and sporadically occurring seizures. Lissencephaly, hydrocephalus, cerebellar deformities, eye abnormalities, and other abnormalities are also linked to it. Although the genetic etiology is  Read More

  • Walker warburg syndrome

    A genetic condition called Walker-Warburg syndrome (WWS) affects how the muscles, brain, and eyes grow. It is the most severe instance of a class of genetic disorders called congenital muscular dystrophies, which result in early-life muscle weakening and atrophy. Walker-Warburg syndrome's warning signs and symptoms appear at birth or in the first few months of life. The majority of those affected by Walker-Warburg  Read More