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Wiedemann–Rautenstrauch (WR) syndrome (German pronunciation: [ˈviːdəman ˈʁaʊtn̩ʃtʁaʊx]), also known as neonatal progeroid syndrome, [1] is a rare autosomal recessive progeroid syndrome. There have been over 30 cases of WR. [2] WR is associated with abnormalities in bone maturation, and lipids and hormone metabolism. [3]
Zespół Wiedemanna-Rautenstraucha (ang. Wiedemann-Rautenstrauch syndrome, neonatal progeroid syndrome), (pol. syndrom progerii noworodkowej) – rzadki zespół wad wrodzonych.
Wiedemann–Rautenstrauch (WR) syndrome, also known as neonatal progeroid syndrome, [91] is an autosomal recessive progeroid syndrome. More than 30 cases have been reported. [92] Most affected individuals die by seven months of age, but some do survive into their teens.
6 sie 2024 · Wiedemann-Rautenstrauch syndrome (WRS), also known as neonatal progeroid syndrome, is a rare genetic disorder. It is characterized by an aged appearance at birth (old man look), growth delays that start before birth (prenatal) and continue after birth, as well as a deficiency or absence of the layer of fat under the skin (subcutaneous lipoatrophy).
Wiedemann-Rautenstrauch syndrome (WDRTS) is a rare autosomal recessive neonatal progeroid disorder characterized by intrauterine growth retardation, failure to thrive, short stature, a progeroid appearance, hypotonia, and variable mental impairment (summary by Toriello, 1990).
2 maj 2023 · Wiedemann-Rautenstrauch syndrome, also known as neonatal progeroid syndrome, starts in the womb, with symptoms of aging apparent at birth. Werner syndrome, also known as adult progeria, begins in the teen years or early adulthood.
6 lis 2019 · Neonatal progeroid syndrome, also known as Wiedemann–Rautenstrauch syndrome, is a rare condition characterized by severe growth retardation, apparent macrocephaly with prominent scalp...
