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impe0096p32 | Bone, Growth Plate and Mineral Metabolism | IMPE2023

Multicentric carpotarsal Osteolysis Syndrome (MCTO) diagnosed in two year old Argentinian girl with mutation de novo in gene MAFB

Ojea Cintia , Maury Fuentes Kelly , Brunetto Oscar , Laura Damia Ana , Bocón Nadia

Background: Multicentric carpotarsal osteolysis syndrome (MCTO) is a rare skeletal disorder commonly caused by MAFB gene mutation. It is characterized by aggressive carpo tarsal osteolysis frequently associated with progressive nephropathy. MAFB negative regulates receptor activator of nuclear factor κB ligand - (RANKL) mediated osteoclast differentiation.Problem: The diagnosis and treatment of MCTO represents a ch...

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impe0096p151 | Sex Differentiation, Gonads and Gynaecology, and Sex Endocrinology | IMPE2023

Argentinian Transgender Children and Adolescents Cohort: an Eight Year Observational Multicenter Study

Figueroa Gacitúa Veronica , Riu Carmen , Esposito Mariela , Rojas Gabriela , Rodriguez saa Magdalena , Carballo Fernanda , Gonzalez Verónica , Biancofiore Nicolas , Maury Fuentes Kelly , Forclaz Veronica , Morin Analia , Fernandez Mentaberry Veronica

Introduction: Transgender and gender–diverse (TGD) individuals do not fully identify with the gender assigned at birth. Argentina has approved in 2012 a pioneer gender identity law (N° 26.743) which depathologize this condition and guarantees access to medical care of TGD individuals. In recent years, there has been a significant increase in the number of youth seeking gender-affirming medical interventions leading to the creation of multidisciplinar...

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IMPE Abstracts

Multicentric carpotarsal Osteolysis Syndrome (MCTO) diagnosed in two year old Argentinian girl with mutation de novo in gene MAFB

Argentinian Transgender Children and Adolescents Cohort: an Eight Year Observational Multicenter Study

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