BACKGROUND:MIRAGE syndrome, a congenital multisystem disorder due to pathogenic SAMD9 variants, describes a constellation of clinical features including 46,XY disorders of sex development (DSD), small for gestational age (SGA) and adrenal insufficiency (AI). It is poorly understood whether SAMD9 variants underlie 46,XY DSD patients born SGA (46,XY DSD SGA) without AI. This study aimed to define the frequency and phenotype of SAMD9 variants in 46,XY DSD SGA without AI. METHODS:Forty-nine Japanese patients with 46,XY DSD SGA (Quigley scale, 2 to 6; gestational age-matched birth weight percentile, <10) without history of AI were enrolled. The single coding exon of SAMD9 was PCR-amplified and sequenced for each patient. Pathogenicity of an iden...
More than 50% of children with severe 46,XY disorders of sex development (DSD) do not have a definit...
International audience17-ß Hydroxysteroid dehydrogenase type 3 (17β-HSD3) is an enzyme transforming ...
Steroidogenic factor-1 (SF-1), also known as nuclear receptor subfamily 5 group A member 1 (NR5A1), ...
Characteristics of the 49 study subjects are shown, including gestational age (A), birth weight SDS ...
Background: Heterozygous de novo variants in SAMD9 cause MIRAGE syndrome, a complex multisystem diso...
IntroductionPrimary adrenal insufficiency (PAI) presenting in the neonatal period can be life threat...
Abstract We describe a case of posthumously diagnosed MIRAGE syndrome (Myelodysplasia, Infection, Re...
Abstract Background Adrenal hypoplasia is a rare congenital disorder, which can be classified into a...
IntroductionMIRAGE syndrome is a rare disease characterized by myelodysplasia, infection, growth res...
It is well established that somatic genomic changes can influence phenotypes in cancer, but the role...
Germline mutations in the SAMD9 and SAMD9L genes, located in tandem on chromosome 7, are associated ...
We report a case of 34 year old woman how has been hospitalized at the age of 6 month with persisten...
A, Western blot analysis showed comparable protein expression levels between wildtype (WT)-SAMD9 and...
Differences in sex development (DSD) in patients with 46,XX karyotype occur by foetal or postnatal e...
Adrenal hypoplasia congenita (AHC) is a rare condition and causes primary adrenal insufficiency. X-l...
More than 50% of children with severe 46,XY disorders of sex development (DSD) do not have a definit...
International audience17-ß Hydroxysteroid dehydrogenase type 3 (17β-HSD3) is an enzyme transforming ...
Steroidogenic factor-1 (SF-1), also known as nuclear receptor subfamily 5 group A member 1 (NR5A1), ...
Characteristics of the 49 study subjects are shown, including gestational age (A), birth weight SDS ...
Background: Heterozygous de novo variants in SAMD9 cause MIRAGE syndrome, a complex multisystem diso...
IntroductionPrimary adrenal insufficiency (PAI) presenting in the neonatal period can be life threat...
Abstract We describe a case of posthumously diagnosed MIRAGE syndrome (Myelodysplasia, Infection, Re...
Abstract Background Adrenal hypoplasia is a rare congenital disorder, which can be classified into a...
IntroductionMIRAGE syndrome is a rare disease characterized by myelodysplasia, infection, growth res...
It is well established that somatic genomic changes can influence phenotypes in cancer, but the role...
Germline mutations in the SAMD9 and SAMD9L genes, located in tandem on chromosome 7, are associated ...
We report a case of 34 year old woman how has been hospitalized at the age of 6 month with persisten...
A, Western blot analysis showed comparable protein expression levels between wildtype (WT)-SAMD9 and...
Differences in sex development (DSD) in patients with 46,XX karyotype occur by foetal or postnatal e...
Adrenal hypoplasia congenita (AHC) is a rare condition and causes primary adrenal insufficiency. X-l...
More than 50% of children with severe 46,XY disorders of sex development (DSD) do not have a definit...
International audience17-ß Hydroxysteroid dehydrogenase type 3 (17β-HSD3) is an enzyme transforming ...
Steroidogenic factor-1 (SF-1), also known as nuclear receptor subfamily 5 group A member 1 (NR5A1), ...