Mevalonate Kinase Deficiency as A Cause of Periodic Fever- A Report of Two Cases
Mevalonate kinase deficiency (MKD) is an exceedingly rare autosomal recessive inborn metabolism error characterized by mutations in the MVK gene, leading to impaired synthesis of cholesterol and isoprenoids. Two case reports of MKD in South India, shedding light on the disease's clinical hetero...
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Main Authors: | Hema Sameera Pinnam (Author), Mahabaleshwar Mamadapur (Author), Sabarinath Mahadevan (Author), Varuni Pragya (Author) |
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Format: | Book |
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Dr. Annil Mahajan,
2024-07-01T00:00:00Z.
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Online Access: | Connect to this object online. |
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