Frasier Syndrome: Decoding Cryptophthalmos syndrome Unraveling the Complexities of This Rare Neurological Condition

What is Frasier Syndrome? Frasier Syndrome, also known as X-linked glomerulopathy, is a rare genetic disorder caused by mutations in the Wilms tumor 1 (WT1) gene located on the X chromosome. This gene plays a key role in kidney development and functions. Mutations in the WT1 gene cause abnormal cell growth and functioning of the kidneys. Sign

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