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Gender dysphoria: when no one is paying attention

Silva, Ricardo; Silva, Ricardo; Santos, Ema

Introduction: Transgender health remains a challenge for healthcare professionals, given the fast evolution of concepts related to gender roles and sexual identity, with frequent updates to definitions and nomenclature. Also, being a delicate and divisive theme in society, it generates distress, suffering, and stigmatization for people experiencing these processes. Besides, there is often significant inaction b...


Imaging clinical case

Cristina, Catarina; Serras, Inês; Santos, Ema; Alves, Rui; Serrano, Dulce

Hirschsprung disease is the most common congenital gut motility disorder and usually diagnosed in the neonatal period. It is caused by an aganglionic bowel segment resulting in absence of intestinal peristalsis and functional obstruction. Diagnosis should be considered in all patients with constipation that does not respond to conventional treatment. Radiography and contrast enema are important diagnostic exams...


Chronic Gastric Volvulus

Santos, Ema; Morão, Sofia; Knoblich, Maria; Alves, Rui


Penile Involvement as Initial Manifestation of Henoch-Schönlein Purpura

Santos, Ema; Henriques, Joana José; Ladeira, Catarina; Alves, Rui


Imaging clinical case

Cristina, Catarina; Serras, Inês; Santos, Ema; Alves, Rui; Serrano, Dulce

Hirschsprung disease is the most common congenital gut motility disorder and usually diagnosed in the neonatal period. It is caused by an aganglionic bowel segment resulting in absence of intestinal peristalsis and functional obstruction. Diagnosis should be considered in all patients with constipation that does not respond to conventional treatment. Radiography and contrast enema are important diagnostic exams...


Poster: NEM TUDO O QUE PARECE É: MULHER 46, XY

Santos, Ema; Fernandes, Pedro F.; Brazão, Kathleen; Santos, Filipa A.; Gromicho, Alexandre; Fernandes, Jorge Lima; Saunders, Duarte; Real, Artur

A síndrome de Insensibilidade Completa aos Androgénios (CAIS) é uma doença recessiva ligada ao cromossoma X causada por mutação no gene do recetor androgénico. É uma patologia do desenvolvimento sexual com uma incidência de 1/20000-100000 nados vivos do sexo masculino. Carateriza-se pela presença de genitais externos femininos em indivíduos 46,XY com testículos criptorquídicos e ausência de resposta a níveis de...


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