ENFERMEDAD DE HARTNUP PDF

7 Sep Transcript of Enfermedad de Hartnup. Abstract Hartnup’s disease is an inherited disorder of metabolism caused by a mutation in the SLC6A (Más información); La pelagra es una enfermedad de deficiencia severa de niacina. .. Pacientes con la enfermedad de Hartnup, un trastorno hereditario que.

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Send this link to let others join your presentation: Add a personal note: Sin embargo, en casos raros, pueden ser graves o potencialmente mortales. Please log in to add your comment. Send the link below via email or IM Copy. The clinical picture is attributed to the inefficient production of nicotinamide and alterations in the synthesis of the neurotransmitter 5-hydroxytryptamine 5-HT caused by decreased absorption of its precursor L-tryptophan W.

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ENFERMEDAD DE HARTNUP by Grupo Psicologia on Prezi

Neither you, nor the coeditors you shared it with will be able to recover it again. The aim of this review is to illustrate the direct link between the disruption in the metabolism of a nutrient elemental and the complex clinical presentation that derives from it.

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Present to your audience Start remote presentation. A firewall is blocking access to Prezi content. Please log in to add your comment. Present to your audience Enfermeddad remote presentation. More presentations by Orlando Marriaga Inmunodeficiencia Secundaria. The characteristic clinical picture of the disease is cerebellar ataxia, pellagra like skin rash related to photosensitivity, aminoaciduria and neuropsychiatric symptoms, commonly depression, irritability and insomnia.

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