Gut dysmotility in children with neurological impairment: the nutritional management

A Corsello, L Scatigno, A Govoni, G Zuccotti… - Frontiers in …, 2023 - frontiersin.org
Intestinal motility disorders represent a frequent problem in children with neurological
impairment. These conditions are characterized by abnormal movements of the gut, which …

ABCD1 gene mutation in an Italian family with X-linkedadrenoleukodystrophy: case series

A Mohn, N Polidori, C Aiello, C Rizzo… - … & metabolism case …, 2021 - edm.bioscientifica.com
Adrenoleukodystrophy is a peroxisomal X-linked recessive disease caused by mutations in
the ABCD1 gene, located on the X-chromosome (Xq28). Gene mutations in patient with …

Adrenoleucodistrofia ligada al cromosoma X. Reporte de caso y revisión de la literatura

P Cueva, JGL Tinitana - Tesla Revista …, 2023 - tesla.puertomaderoeditorial.com.ar
Esta revisión, presenta un caso clínico poco frecuente en el contexto actual, como lo es la
adrenoleucodistrofia. La adrenoleucodistrofia (ADL) es un raro trastorno peroxisomal el cual …

Educational Case: Adrenocortical insufficiency—Causes and pathogenesis

SJ Vance, JT Horsley, MP Welch… - Academic …, 2022 - academicpathologyjournal.org
Educational Case: Adrenocortical insufficiency—Causes and pathogenesis - Academic
Pathology Skip to Main Content Skip to Main Menu Advertisement Academic Pathology Submit …

Adrenoleucodistrofia ligada al cromosoma X. Reporte de caso

PJ Cueva Jiménez - 2023 - dspace.ucacue.edu.ec
Background: This review presents a rare clinical case of adrenoleukodystrophy in the
current context. Adrenoleukodystrophy (ADL) is a rare peroxisomal disorder which is X …

[PDF][PDF] Daniela Rabelo* Andrea De Gois

N Monsores - researchgate.net
Rare diseases are crossed by particularities and unique experiences of biological
constitution level, social reality and experience of illness. This study is the first passage to …