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Introduction: Neurofibroma, a rare benign tumor of the peripheral nervous system, can manifest anywhere along a nerve from the dorsal ganglion to its terminal branches. Myxoid neurofibroma can present as a solitary non-tender nodule and is often confirmed by positive immunohistochemical staining for S-100 protein. However, in 50% of cases, neurofibromas are associated with neurofibromatosis.

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Article Synopsis
  • Waardenburg syndrome (WS) is a genetic disorder that leads to pigment abnormalities and hearing loss, and this case report discusses a rare instance in a preterm infant who had multiple congenital anomalies.
  • The baby, born at 35 weeks, showed classic WS features like a white forelock and required intensive care for respiratory and feeding issues, along with further complications involving his heart and kidneys.
  • The report emphasizes the need for multidisciplinary care and early intervention to improve outcomes for infants with WS, especially highlighting the unexpected presence of cardiac and renal anomalies in this case.
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