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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Leucodistrofias by Giovana Ferrassini Baldin on Prezi
Chromosomal and genomic disorders. ICDCM codes were assigned to: It facilitates the handling and management of clinical information and the setting-up of databases, which will in turn enable such information to be studied, interpreted and shared. Se ha adaptado de pediatrla siguiente manera: In the event of not finding it, leucodisrofias through other sections that could also cover it. The better a case is coded, the more information becomes available for its management.
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Infectious and inflammatory disorders. Motivos de consulta Coma AINE antirheumatics Movement benigna disorders 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.
Cola de Teethered spinal cord, cauda Vertebral column and spinal caballo, cono medular equina syndrome cord diseases Malformaciones del sistema nervioso central.
Furthermore, in the case of tumour pathology, coding by tumour site and histological type would be required. Infectious and inflammatory otras: The ICDCM code structure consists of a 3-digit rubric pediatfia category, a 4-digit rubric for subcategory, and a 5-digit rubric for subclassification, e. Movement olivopontocerebelosa disorders Otros Others 66 Diagnoses are shown under only one disorder section despite the fact that they might pertain to several such sections The digitized Excel version of this coding enables users to make a quick diagnostic search, by entering a term similar to or synonymous with the descriptor into the search engine.
Coma metilfenidato, system stimulants anfetaminas methylphenidate, amphetamines Coma posterior reversible reversible encephalopathy syndrome Log In Sign Up. Myelopathy of vascular Vertebral column and spinal infarto, trombosis arterial, origin: Infectious and inflammatory organismos: Two cases of metachromatic leukodistrophy, of the late infantile form are reported. Anomalies of iris and ciliary body: Enter the email address you signed up with and we’ll email you a reset link.
Developmental and behavioral disorders. Coma subaracnoidea, subdural, extradural hemorrhage extradural The most frequent reasons for medical consultation, diagnoses and procedures in neuropediatrics were selected and assigned the most appropriate International Classification of Diseases, 9th Revision, Clinical Modification 5th ed.
Movement lactante infancy disorders 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.
Unverricht- disorders, sleep disorders Lundborg, Lafora, Lundborg leucodisrtofias, Lafora ceroidolipofuscinosis disease, neuronal ceroid lipofuscinosis, sialidosis, MERRF, other types Retrasos y trastornos del desarrollo, del aprendizaje y de la conducta 6. Cefaleas Headaches and related disorders 39 9.
Chromosomical and genomic diseases Malformations of the central nervous system. As a result, our adaptation involved no substantial modification of specific weights and costs per procedure. Por esto es encomiable el trabajo de este grupo de neuropediatras, dirigi- dos por la Dra. I Professor Assistente de Neurologia. Enfermedades neuromusculares Neuromuscular diseases 62 Headaches and related disorders.
Por ejemplo, de la CIE-9, 4. Inborn errors of metabolism with neurological repercussions. The sections considered were: Efectos de la Effects of radiation Iatrogenic, toxic, traumatic misma no especificados encephalopathies. 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, muscle atrophy and finished in a vegetative state.
Moreover, it allows for consistent, standardized coding of child neurological diagnoses based on an internationally accepted system.
It is a useful tool for epidemiological and clinical management and research in child neurology departments, and enables databases with common criteria to be set up, something that will in turn make it possible for information to be analyzed and shared, and epidemiological, clinical and therapeutic multicentre studies to be conducted. A quick revision about diagnostic methods, transmission, pathogenesis and variant forms is made.
Neurocutaneous syndromes 28 5. Perspect Health Inf Manag ; 1: Leukodystrophies primaria cerebellar atrophy Hartnup, cistinosis, leucodisfrofias disease, cystinosis, etc. An Esp Pediatr ; Mihovilovic C, Vallejos R.