Ogden syndrome - Wikipedia
Ogden syndrome, also known as N-terminal acetyltransferase deficiency (NATD), [1] is an X-linked disorder of infancy comprising a distinct combination of distinctive craniofacial features producing an aged appearance, growth failure, hypotonia, global developmental delays, cryptorchidism, and spontaneous cardiac arrhythmias.
Ogden Syndrome - Symptoms, Causes, Treatment | NORD
Mar 29, 2024 · Ogden syndrome is a rare genetic condition characterized by a spectrum of clinical features, including facial differences, aged appearance, developmental disabilities, skeletal anomalies, genitourinary anomalies, irregular heartbeat (cardiac arrhythmia) and other conditions.
Ogden syndrome | About the Disease | GARD - Genetic and Rare …
Ogden syndrome is a rare, genetic progeroid syndrome characterized by a variable phenotype including postnatal growth delay, severe global developmental delay, hypotonia, non-specific dysmorphic facies with aged appearance and cryptorchidism, as well as cardiac arrthymias and skeletal anomalies.
Ogden syndrome - National Organization for Rare Disorders
Ogden syndrome is a rare, genetic progeroid syndrome characterized by a variable phenotype including postnatal growth delay, severe global developmental delay, hypotonia, non-specific dysmorphic facies with aged appearance and cryptorchidism, as well as cardiac arrthymias and skeletal anomalies.
Confirmation of Ogden syndrome as an X‐linked recessive fatal …
Ogden syndrome is a rare lethal X‐linked recessive disorder caused by a recurrent missense variant (Ser37Pro) in the NAA10 gene, encoding the catalytic subunit of the N‐terminal acetyltransferase A complex (NatA).
Nonprofit Organization for Ogden Syndrome| Ogden CARES
Ogden CARES is a nonprofit foundation providing education and financial support for individuals affected by Ogden Syndrome/NAA10. Reach out to us today.
Pharos : Disease Details - Ogden syndrome - National Institutes …
Ogden syndrome is a rare, genetic progeroid syndrome characterized by a variable phenotype including postnatal growth delay, severe global developmental delay, hypotonia, non-specific dysmorphic facies with aged appearance and cryptorchidism, as well as cardiac arrthymias and skeletal anomalies.
Ogden Syndrome is caused by a single spelling error on the crucial NAA10 gene. NAA10 is a protein coding gene essential for normal cell function. NAA10 encodes the enzyme known as N-Terminal-Acetyltransferase 10 which along with NAA15 makes up the NatA complex.
Ogden syndrome - NIH Genetic Testing Registry (GTR) - NCBI
Ogden syndrome (OGDNS) is an X-linked neurodevelopmental disorder characterized by postnatal growth failure, severely delayed psychomotor development, variable dysmorphic features, and hypotonia. Many patients also have cardiac malformations or arrhythmias (summary by Popp et al., 2015).
Orphanet: Ogden syndrome
Ogden syndrome is a rare, genetic progeroid syndrome characterized by a variable phenotype including postnatal growth delay, severe global developmental delay, hypotonia, non-specific dysmorphic facies with aged appearance and cryptorchidism, as well as cardiac arrthymias and skeletal anomalies.
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