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From RYR-1 Diagnosis To Heading Home: Baby Charlie's Journey With The Rare Condition
Автор: Blythedale Children's Hospital
Загружено: 2023-10-25
Просмотров: 2392
Описание: Four-month-old Charlie was born with Ryanodine Receptor 1 Related (RYR-1) Myopathy, a rare genetic disorder that disrupts the flow of calcium in muscle cells, limiting the muscle's ability to contract. Diagnosed with low muscle tone at birth, Charlie was transferred from the NICU to Blythedale Children's Hospital for comprehensive rehabilitation and feeding therapy.
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