HARTNUP DISEASE OVERVIEW HARTNUP disease, a rare genetic disorder, has long puzzled medical experts with its complex array of symptoms and challenges in diagnosis. However, recent advancements in understanding this condition have shed light on its underlying mechanisms, offering hope for effective treatment strategies. In this article, we will delve into the enigmatic world of […]
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Treacher-Collins Syndrome (TCS) A hereditary condition called Treacher-Collins Syndrome (TCS) impairs the growth of the bones and other tissues of the face, giving rise to unusual facial traits. People with TCS frequently have undeveloped cheekbones, which can give the appearance that their faces are sunken. The ears of those with TCS may be tiny, malformed,
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Turner Syndrome: Causes, Symptoms, Diagnosis, and Treatment Itis a genetic disorder that affects females. It occurs when one of the two X chromosomes is partially or completely missing. Instead of having the usual 46 chromosomes, women with Turner Syndrome have only 45 chromosomes, with only one X chromosome instead of two. The syndrome is named
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