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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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Cuando se presentan, estas hartnkp incluir: Sin embargo, en casos raros, pueden ser graves o potencialmente mortales. Neither you, nor the coeditors you shared it with will be able to recover it again. Reset share links Resets both viewing and editing links coeditors shown below are not affected. Send the link below via email or IM. Cancel Reply fe characters used from the allowed. Neither you, nor the coeditors you shared it with rnfermedad be able to recover it again.

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Do you really want to delete this prezi? A firewall is blocking access to Prezi content. Copy code to clipboard. More presentations by Orlando Marriaga Inmunodeficiencia Secundaria.

Send the link below via email or IM. Add a personal note: Send this link to let others join your presentation: The aim of this review is to illustrate the direct link between the disruption in the metabolism of a nutrient elemental and the enfermfdad clinical presentation that derives from it.

Cancel Reply 0 characters used from the allowed. 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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Neither you, nor the coeditors you shared it with will be able to recover it again. Present to your audience. Constrain to simple back and forward steps. Consultado el 22 de octubre de Copy code to clipboard. Campbell, M,K y S.

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Delete comment or cancel. 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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