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There is a particular type of GLP-1 telehealth provider that gets overlooked in most comparison articles: the one that actually bothers to put board-certified obesity medicine specialists in the room

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Alterations in these genes result in shortening of telomeres, which in turn leads to defects in proliferation and spontaneous chromosomal rearrangements.[199] Levels of TERC, the RNA component of the telomerase complex, are reduced in all dyskeratosis congenita patients.[200] Missense pathogenic variants in WRAP53 , a gene with a protein product that facilitates trafficking of telomerase, have also been associated with an autosomal recessive form of dyskeratosis congenita.[201] Pathogenic variants in C16orf57 were identified in 6 of 132 families who did not have a variant detected in other known genes.[202] C16orf57 pathogenic variants are also associated with poikiloderma with neutropenia.[203] For more information about poikiloderma congenitale, see the Rothmund-Thomson syndrome section

In adults, these defects are usually characterized by the accumulation of medium-chain and long-chain (3-hydroxy) carnitine derivatives, and they are associated with lipotoxicity in several organs that can lead to life-threatening complications and comorbidities

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[5] [6] Eye neoplasms can affect all parts of the eye, and can either be benign (noncancerous) or malignant (cancerous), in which case it is known as eye cancer