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Metabolism - MedlinePlus Genetics

Summarized by Plex Scholar
Last Updated: 11 October 2021

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Farber lipogranulomatosis

Farber lipogranulomatosis is a rare inherited condition involving the malfunction and use fats in the body. Three classic signs take place in Farber lipogranulomatosis: a hoarse voice or a weak cry, small lumps of fat under the skin and in various other cells, and painful and inflamed joints. Impacted individuals might have difficulty breathing, an enlarged liver and spleen, and developmental delay. Researchers have defined seven sorts of Farber lipogranulomatosis based on their particular features. Babies birthed with type 1 Farber lipogranulomatosis generally endure only into very early childhood years. Types 2 and 3 normally have much less severe symptoms and signs than the other types. Kids with these sorts of Farber lipogranulomatosis commonly live into mid- to late childhood years. Children with type 5 Farber lipogranulomatosis survive into very early childhood. Types 6 and 7 are very rare, and affected people have other linked conditions in enhancement to Farber lipogranulomatosis.

Source link: https://medlineplus.gov/genetics/condition/farber-lipogranulomatosis

* Please keep in mind that all text is summarized by machine, we do not bear any responsibility, and you should always check original source before taking any actions

* Please keep in mind that all text is summarized by machine, we do not bear any responsibility, and you should always check original source before taking any actions