Anales de Pediatría clínica consiste en malabsorción de nutrientes y electrólitos, junto con esteatorrea y diarrea que dificultan el desarrollo ponderoestatural. Anales de Pediatría · Volume 58, Issue 6, , Pages open access Déficit de vitaminas liposolubles. Acantocitosis. Esteatorrea. Malabsorción. Motilidad, flujo intestinal y patrón de ácidos biliares en niños con síndrome diarreico. Article (PDF Available) in Revista chilena de pediatría 48(1) · February .

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Chronic idiopathic intestinal pseudo-obstruction. J Pediatr Gastroenterol Nutr ; The use of new manometric tecniques and specific histological procedures have allowed to clarify the pathogenesis of some of these entities including mitochondrial diseases and paraneoplasic syndromes.

Familial hypobetalipoproteinemia caused by a mutation in the apolipoprotein B gene that results in a truncated species of apolipoprotein B.

Basically, the failure of the intestinal motility is a consequence of muscular disorder, neurological disorder or both.

Krishnamurthy S, Schuffler MD. Neuromuscul Disord ; 2: Familial lipoprotein abetalipoproteinaemia, hypobetalipoproteinaemia esheatorrea Tangier disease. Algunos casos pueden ser primarios en su origen 8, Neurol Clin ; Keller J, Layer P.


Arch Dis Child, 54pp. Jejunal manometry in distal subacute mechanical obstruction: SJR uses a similar algorithm as the Google page rank; it provides a quantitative and qualitative measure of the journal’s impact.

SRJ is a prestige metric based on the idea that not all citations are the same. Pathology of neuromuscular disorders of the small intestine and colon. To improve our services and products, we use “cookies” own or third parties authorized to show advertising related to client preferences through the analyses of navigation customer behavior.

Parasitosis intestinales en Pediatría by Gladymar Pérez on Prezi

Clinical characteristics of chronic idiopathic intestinal pseudo-obstruction in adults. J Clin Gastroenterol ; Clinical and laboratory features, therapeutic manipulations, and follow-up study of three members of a Greek family. Apolipoprotein genetic variation and human disease. Small intestinal bacterial overgrow: Neurogastroenterol Motil ; Advances in our understanding of the pathology of chronic intestinal pseudo-obstruction.

Subscribe to our Newsletter. Blood, 5pp. Los pacientes con esclerodermia eesteatorrea mueren como consecuencia de complicaciones renales, cardiacas o digestivas.


Histological phenotypes of enteric smoth muscle disease causing functional intestinal obstruction in chilhood. Seminars in Medicine of the Beth Israel Hospital.

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Los efectos extrapiramidales de la primera hacen que no puedan administrarse dosis altas de la misma. Significant biochemical alterations reduced levels of triglicerides, cholesterol, and vitamin A and absence of apolipoprotein B and vitamin E led to the diagnosis of homozygous hypobetalipoproteinemia, which was subsequently confirmed by genetic studies.

Metabolic basis of inherited disease. Outcome of colectomy for slow transit constipation in relation to presence of small-bowel dysmotylity.

Importance of small bowel manometry. Gastric electrical stimulation for medically refractory gastroparesis.

Dig Dis Sci ; Full text is only aviable in PDF. Am J Roentgenol ; A esgeatorrea mitochondrial mutation associated with prominent inicial gastrointestinal symptoms and progressive encephaloneuropathy.

Ann N Y Acad Sci,pp.