16th-century English MP stubs

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Progeria is an extremely rare autosomal dominant genetic disorder in which symptoms resembling aspects of aging are manifested at a very early age. Progeria is one of several progeroid syndromes. Those born with progeria typically live to their mid-teens to early twenties. It is a genetic condition that occurs as a new mutation and is rarely inherited, as carriers usually do not live to reproduce children. Although the term progeria applies, strictly speaking, to all diseases characterized by premature aging symptoms, it is often used specifically in reference to Hutchinson–Gilford progeria syndrome (HGPS). Severe cardiovascular complications usually develop by puberty, resulting in death.

Woodhouse–Sakati syndrome

Progeria

1619 (MDCXIX) was a common year starting on Tuesday of the Gregorian calendar and a common year starting on Friday of the Julian calendar, the 1619th year of the Common Era (CE) and Anno Domini (AD) designations, the 619th year of the 2nd millennium, the 19th year of the 17th century, and the 10th and last year of the 1610s decade. As of the start of 1619, the Gregorian calendar was 10 days ahead of the Julian calendar, which remained in localized use until 1923.

Parliament of England (pre-1707) MP stubs

Woodhouse–Sakati syndrome, is a rare autosomal recessive multisystem disorder which causes malformations throughout the body, and deficiencies affecting the endocrine system.

Sir John Brocket (c. 1540 – 2 October 1598) of Brocket Hall in Hertfordshire was an English politician.

Progeria is an extremely rare autosomal dominant genetic disorder in which symptoms resembling aspects of aging are manifested at a very early age. Progeria is one of several progeroid syndromes. Those born with progeria typically live to their mid-teens to early twenties. It is a genetic condition that occurs as a new mutation and is rarely inherited, as carriers usually do not live to reproduce children. Although the term progeria applies, strictly speaking, to all diseases characterized by premature aging symptoms, it is often used specifically in reference to Hutchinson–Gilford progeria syndrome (HGPS).

John Brocket (died 1598)