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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]
- Progeroid Syndromes
Wiedemann–Rautenstrauch (WR) syndrome, also known as...
- Progeria
Progeroid syndromes are a group of diseases that cause...
- Progeroid Syndromes
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.
Progeroid syndromes are a group of diseases that cause individuals to age faster than usual, leading to them appearing older than they actually are. People born with progeria typically live until their mid- to late-teens or early twenties.
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).
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...
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 veins, and lipodystrophy. It is caused by biallelic variants in POLR3A, a gene encoding for a subunit of RNA polymerase III.
