Tag: KOS
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Singapore Family Faces Rare Genetic Disorder: A Daughter’s Fight with Kaufman Oculocerebrofacial Syndrome
Introduction: A Silent Birth and a Silent Struggle When Rania Safiyya Ridzwan was born in 2020 in Singapore, the delivery room was unusually quiet. She did not cry, and her mother, Madam Sri Syazwani Mohd Yazid, recalls a scene that would foreshadow a challenging journey ahead. What began as a routine birth soon revealed a…
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Singapore Family Faces Rare Genetic Disorder KOS: A Mother’s Courage and Medical Insight
Introduction to a rare diagnosis In 2020, a Singaporean family welcomed their daughter, Rania, with a quiet start to life. The newborn did not cry, and her initial signs were subtle but concerning, prompting a rapid medical response. What followed was a complex medical journey that would reveal a rare genetic condition known as Kaufman…
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Lives Shaped by a Rare Genetic Disorder: A Singapore Family’s Battle with Kaufman Oculocerebrofacial Syndrome
Introduction: A Silent Beginning and a Hidden Diagnosis When Rania Safiyya Ridzwan was born in 2020, the delivery room felt unusually quiet. She did not cry, a sign that something was amiss, and the newborn’s first moments required urgent attention in the neonatal intensive care unit. Her mother, Madam Sri Syazwani Mohd Yazid, recalls the…