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May 2, 2023 · Progeria is a rare genetic disorder that causes children to age rapidly, with symptoms such as slowed growth, hair loss and heart problems. Learn about the causes, diagnosis and treatment of progeria, and how it differs from other progeroid syndromes.
Progeria is a specific type of progeroid syndrome, also known as Hutchinson–Gilford syndrome or Hutchinson–Gilford progeroid syndrome (HGPS). A single gene mutation is responsible for causing progeria.
- Lonafarnib
- Growth delay, short height, small face, hair loss
- Genetic
- Mostly symptomatic
Dec 7, 2022 · Progeria is a fatal condition that causes children to age prematurely. Learn about the symptoms, causes, diagnosis, treatment and outlook of this rare disorder.
Dec 8, 2022 · Progeria is a rare genetic condition that causes rapid or early aging in children or adults. Learn about the two main types of progeria, HGPS and Werner syndrome, and how they are diagnosed, treated, and inherited.
Dec 27, 2013 · Progeria is an extremely rare genetic disease of childhood characterized by dramatic, premature aging. The condition, which derives its name from "geras," the Greek word for old age, is estimated to affect one in 4 million newborns worldwide.
May 2, 2023 · Progeria is a rare genetic condition that causes rapid aging and early death. Learn about the symptoms, diagnosis, treatment options and coping strategies for children and families with progeria.
Sep 5, 2022 · Progeria is a disease that makes children age rapidly and die young. Learn about the causes, symptoms, diagnosis, and treatments of this condition, and how it differs from similar syndromes.
