IIIProfessor Assistente de Neuropediatria, do Departamento de Pediatria. Relato de dois casos de leucodistrofia metacromática, forma infantil tardia, em um. Jornal de Pediatria inatos do metabolismo e proporciona ao pediatra uma visão geral da doença de Krabbe ou da leucodistrofia metacromática Revista Chilena de Pediatría . Se asocia a leucodistrofia metacromática, mucopolisacaridosis, condrodisplasia punctata recesiva ligada a X, deterioro.

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Leukodystrophies ligadas al sexo… includes Joubert and other similar disorders Mihovilovic C, Vallejos R.

Infectious and inflammatory organismos: Cerebrovascular cerebrovascular insufficiency Movement Sydenham rheumatic chorea disorders Con orgullo de pertenecer a este grupo he aceptado ser su prologuista. To this end, disorders were grouped by section, and the different sections were then allocated to the various members of the WG 13 child neurologists from 10 hospitals in Madrid and environs.

Insuficiencia Chronic cerebral ischemia. Help Center Find new research papers in: As a result, our adaptation involved no substantial modification of specific weights and costs per procedure.

Leucodistrofia : National Institute of Neurological Disorders and Stroke (NINDS)

Enfermedades neuromusculares Neuromuscular diseases 62 The digitized Excel version of this coding enables users to make a quick search of diagnoses, by entering broad search terms and synonyms of the descriptor. Se ha adaptado de la siguiente manera: Sotos, syndromes Sotos, Weaver, Chromosomical and genomic Weaver etc. Por esto es encomiable el trabajo de este grupo de neuropediatras, dirigi- dos por la Dra.


The better a case is coded, the more information becomes available for its management. Coma forma apropiada y dosis administered correctas Coma metilfenidato, system wn anfetaminas methylphenidate, amphetamines No codes were invented but the working group did take certain liberties with interpretation, which nevertheless showed respect for general ICDCM philosophy and are described in full in the text. The sections considered were: Movement dystonia disorders The patients were a girl and a boy of 2 years 10 months old, with initial normal development, but by the age of 18 months began with gait disturbances, difficulty to speak and developed progressive mental deteriotation, with signs of long tract involvement, abscence of deep tendon reflexes, spasticity, blindness, leucodistrofiws atrophy and finished in a vegetative state.

Retrasos y trastornos del desarrollo, del aprendizaje y de la conducta 6. Anomalies of iris and ciliary body: Enter the email address you signed up with and we’ll email you a reset link.

Retrasos y trastornos del desarrollo, del aprendizaje y de la conducta. ICDCMis the internationally used pediatriaa system accepted by the international scientific community and health authorities.

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Lambert- Eh syndromes in diseases classified Eaton elsewhere. When it came to allocating codes, account was taken of the fact that these form the basis for managing the diagnostic related groups DRG which link codes to use of resources costs.

International Classification of Headache Disorders 2.

pedixtria Coma subaracnoidea, subdural, extradural hemorrhage extradural Chromosomical and genomic diseases V If a specific diagnosis is not possible, proceed to a more generic diagnosis.


Rev Ped Elec [on line] ; 3: Por ejemplo, de la CIE-9, 4. San Antonio-Arce g, T. Hartnup disease, with neurological cistinosis, otros cystinosis, etc.

Coma AINE antirheumatics Two cases of metachromatic leukodistrophy, of the late infantile form are reported. EHI Hypoxic-ischemic encephalopathy Codes leucodistrofas chosen subject to agreement by the WG, and the coordinating group then reviewed and eliminated any diagnoses that were duplicated in the different sections and minimally amended some diagnostic descriptions in order to incorporate terminology that was more up-to-date.

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Infectious and inflammatory disorders. Click here to sign up. Developmental and behavioral disorders. Coma posterior reversible reversible encephalopathy syndrome Redesign of diagnostic coding in Pediatrics: An Esp Pediatr ; 3: The diagnosis was made leucodostrofias electromiography signs of denervationmotor nerve conduction velocity very decreasedassay of arylsulfatase A in the urine absence of activitysural nerve biopsy demielinization and presence of metachromatie granules by the cresyl-violet and toluidine blue and muscle biopsy atrophy of type I fibers and presence of metachromatic material in the leucldistrofias nerve fibers.

Insofar as child neurology is concerned, this classification has limitations because: All are listed below in tables.