We report a case of Hutchinson-Gilford progeria syndrome (HGPS). The patient showed the
characteristics of scleredema at the age of 2.5 months but developed all the manifestations …

Hutchinson–G ilford progeria syndrome (HGPS) is a rare, uniformly fatal, premature aging
disease with distinct dermatologic features. We sought to identify and describe the initial skin …

We present a 7-week-old male infant with pseudoscleroderma as a primary manifestation of
the Hutchinson-Gilford syndrome of premature aging. He had suffered intra-uterine growth …

We describe evolving dermatologic findings in a male with progeria from age 1 month to
21.5 months. At 18 months of age, irregular pigmentary changes of the abdomen, early …

Hutchinson-Gilford progeria syndrome is an extremely rare condition with features of
premature and accelerated aging. The pattern of inheritance is unclear, although both …

Progeria, also known as Hutchinson-Gilford syndrome, is an extremely rare, severe genetic
condition wherein symptoms resembling aspects of aging are manifested at an early age. It …

Progeria infantum (Hutchinson–Gilford syndrome) is a very rare syndrome of premature
aging characterized by growth retardation and specific, progressive, premature senescent …

We report on a 35‐week gestation female fetus with Hutchinson‐Gilford progeria (HGP).
This patient, who is the first reported with neonatal HGP in the English literature but is the …

Abstract Hutchinson–Gilford Progeria Syndrome is a rare genetic disorder characterized by
premature aging involving the skin, bones, heart, and blood vessels. We report a three-year …

Hutchinson–Gilford progeria syndrome is a rare genetic disorder characterized by
premature aging of the skin, bones, heart, and blood vessels. We report a 6‐year‐old boy …