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.
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.
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).
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.
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.
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).
Ogden syndrome (Concept Id: C3275447) - National Center for ...
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).
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