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Is your child not crawling? They could have THIS rare disease
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Is your child not crawling? They could have THIS rare disease

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          🞛 This publication is a summary or evaluation of another publication 🞛 This publication contains editorial commentary or bias from the source
Early diagnosis of rare diseases like Spinal Muscular Atrophy (SMA) is crucial for managing symptoms and improving quality of life. Symptoms like diff
The article from the Times of India discusses a rare genetic disorder known as Congenital Muscular Dystrophy (CMD), which can affect infants' ability to crawl. CMD leads to muscle weakness and atrophy from birth or early infancy, impacting motor skills like crawling, standing, and walking. Symptoms might also include joint contractures, scoliosis, and respiratory issues. The article highlights that while CMD is rare, early diagnosis through genetic testing and clinical evaluation is crucial for managing the condition. Treatment focuses on supportive care, physical therapy, and sometimes, surgical interventions to improve quality of life. Awareness about such conditions is vital as they can often be misdiagnosed or overlooked due to their rarity.

Read the Full Indiatimes Article at:
[ https://timesofindia.indiatimes.com/life-style/health-fitness/health-news/is-your-child-not-crawling-they-could-have-this-rare-disease/articleshow/115853196.cms ]