CellWell record HH-282515
Current Diagnosis and Management of Familial Hypobetalipoproteinemia 1
Tetsuji Wakabayashi; Manabu Takahashi; Hiroaki Okazaki; Sachiko Okazaki; Koutaro Yokote; Hayato Tada; Masatsune Ogura; Yasushi Ishigaki; Shizuya Yamashita; Mariko Harada-Shiba
2024
In plain language
This review describes familial hypobetalipoproteinemia 1 as a rare, codominantly inherited disorder caused by APOB gene defects that disable formation of the lipoproteins needed to carry cholesterol, triglycerides and fat-soluble vitamins.
- Evidence
- Emerging
- Design
- Primary research (design unspecified)
Cite this record: https://thecellwell.org/studies/HH-282515
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