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SPG11 is associated with BMI changes and hypothalamic damage

SPG11 mutations are the most relevant cause of autosomal recessive Hereditary Spastic Paraplegia(HSP). Patients present with marked weight gain, which contrasts from caquexia generally observed in other neurodegenerative disorders. We have chosen to evaluate the hypothalamus as it is an important CN...

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Bibliographic Details
Main Authors:	Hernández, Ana, Junior, Marcondes Franca, Faber, Ingrid, Martinez, Alberto, Rezende, Thiago
Format:	Online
Language:	Portuguese
Published:	Universidade Estadual de Campinas 2019
Subjects:	SPG11 BMI Neuroimaging
Online Access:	https://econtents.sbu.unicamp.br/eventos/index.php/pibic/article/view/2200
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