Hirschsprung's disease is a condition characterized by the absence of ganglion cells in a variable segment of the large intestine, mainly producing the symptom of constipation and being usually diagnosed in the first year of life. With diagnostic methods already established in the literature, the sole treatment is surgery. The objective of this study is to report a case of late diagnosis of the disease at age 13, with symptoms of fecal incontinence in its evolution. Resumo: A Doença de Hirschsprung é uma patologia caracterizada pela ausência de células ganglionares em um segmento variável do intestino grosso, produzindo principalmente o sintoma de constipação, sendo normalmente diagnosticada até o primeiro ano de vida. Com métodos diagnósti...
Hirschsprung's disease (HD) is a congenital anomaly of innervation of the lower intestine, limited t...
Hirschsprung's disease (HD) is a congenital anomaly of innervation of the lower intestine, limited t...
Hirschsprung's disease is characterized by absence of ganglion cells in submucosal and myenteric ple...
AbstractHirschsprung's disease is a condition characterized by the absence of ganglion cells in a va...
ABSTRACTHirschsprung's disease is a condition characterized by the absence of ganglion cells in a va...
Trabalho Final do Curso de Mestrado Integrado em Medicina, Faculdade de Medicina, Universidade de Li...
Trabalho Final do Curso de Mestrado Integrado em Medicina, Faculdade de Medicina, Universidade de Li...
Orientador: Luiz Fernando Bleggi TorresCo-orientador Jose Ederaldo Queiroz TellesDissertação (mestra...
Hirschsprung’s disease is an important cause of intestinal obstruction or constipation in newborns a...
Hirschsprung disease is a disease that attacks the human digestive system, mainly in the large<br />...
Hirschsprung’s disease (HD), or congenital megacolon, is a disease characterized by the absence of g...
Hirschsprung’s disease (HD) is uncommon, and most of the cases occur in neonates. It is rarely diagn...
Congenital intestinal aganglionosis, also called Hirschsprung disease (HD), is defined as the absenc...
Congenital intestinal aganglionosis, also called Hirschsprung disease (HD), is defined as the absenc...
To describe the case of an infant with Hirschsprung's disease presenting as total colonic agangliono...
Hirschsprung's disease (HD) is a congenital anomaly of innervation of the lower intestine, limited t...
Hirschsprung's disease (HD) is a congenital anomaly of innervation of the lower intestine, limited t...
Hirschsprung's disease is characterized by absence of ganglion cells in submucosal and myenteric ple...
AbstractHirschsprung's disease is a condition characterized by the absence of ganglion cells in a va...
ABSTRACTHirschsprung's disease is a condition characterized by the absence of ganglion cells in a va...
Trabalho Final do Curso de Mestrado Integrado em Medicina, Faculdade de Medicina, Universidade de Li...
Trabalho Final do Curso de Mestrado Integrado em Medicina, Faculdade de Medicina, Universidade de Li...
Orientador: Luiz Fernando Bleggi TorresCo-orientador Jose Ederaldo Queiroz TellesDissertação (mestra...
Hirschsprung’s disease is an important cause of intestinal obstruction or constipation in newborns a...
Hirschsprung disease is a disease that attacks the human digestive system, mainly in the large<br />...
Hirschsprung’s disease (HD), or congenital megacolon, is a disease characterized by the absence of g...
Hirschsprung’s disease (HD) is uncommon, and most of the cases occur in neonates. It is rarely diagn...
Congenital intestinal aganglionosis, also called Hirschsprung disease (HD), is defined as the absenc...
Congenital intestinal aganglionosis, also called Hirschsprung disease (HD), is defined as the absenc...
To describe the case of an infant with Hirschsprung's disease presenting as total colonic agangliono...
Hirschsprung's disease (HD) is a congenital anomaly of innervation of the lower intestine, limited t...
Hirschsprung's disease (HD) is a congenital anomaly of innervation of the lower intestine, limited t...
Hirschsprung's disease is characterized by absence of ganglion cells in submucosal and myenteric ple...