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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, neonatal progeroid syndrome), (pol. syndrom progerii noworodkowej) – rzadki zespół wad wrodzonych. Objawia się wewnątrzmacicznym zahamowaniem wzrostu, niską masą urodzeniową, niezrośniętymi szwami czaszkowymi, upośledzeniem umysłowym i charakterystyczną dysmorfią twarzy związaną z zanikiem ...
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]
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).
Wiedemann-Rautenstrauch syndrome is a rare genetic syndrome characterized by an aged appearance at birth. Other signs and symptoms include intrauterine growth restriction, feeding difficulties, distinctive craniofacial features, hypotonia, developmental delay, and mild to severe intellectual disability.
Learn about Wiedemann-Rautenstrauch syndrome, a type of progeria that causes rapid aging in infants and children. Find out the signs, symptoms, causes, inheritance, and resources for this rare condition.
Wiedemann-Rautenstrauch syndrome. A rare multiple congenital anomalies/dysmorphic syndrome characterized by marked prenatal and postnatal growth retardation, decreased subcutaneous fat, hypotrichosis, relative macrocephaly and an unusual face. Mild to moderate intellectual disability is common.
