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Codificación en Neurología Pediátrica (CIE-9) - Revista de Neurología

Codificación en Neurología Pediátrica (CIE-9) - Revista de Neurología

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17. Enfermeda<strong>de</strong>s neuromusculares<br />

17. Neuromuscular diseases<br />

<strong>CIE</strong>-9/<br />

ICD-9<br />

64<br />

CE/<br />

SC<br />

Diagnóstico Diagnose<br />

357.82 S/E Polineuropatía <strong>de</strong>l <strong>en</strong>fermo crítico Critical illness polyneuropathy<br />

357.9 S/E Polineuropatía no especificada Polyneuropathy, unspecified<br />

358.0 S/E Miast<strong>en</strong>ia grave Myasth<strong>en</strong>ia gravis<br />

358.1 S/E Miast<strong>en</strong>iformes (síndromes). Lambert-<br />

Eaton<br />

359.0 S/E Miopatía congénita (c<strong>en</strong>tral core,<br />

nemalínica, multicore, miotubular,<br />

c<strong>en</strong>tronuclear, <strong>de</strong>sproporción congénita<br />

<strong>de</strong> fibras…)<br />

359.1 01 Distrofia <strong>de</strong> cinturas (sarcoglicanopatías,<br />

calpeinopatías...)<br />

359.1 02 Distrofia facioescapulohumeral (Landouzy-<br />

Dejerine)<br />

Myasth<strong>en</strong>ic syndromes in diseases classified<br />

elsewhere. Eaton-Lambert syndrome<br />

Cong<strong>en</strong>ital myopathies (c<strong>en</strong>tral core,<br />

minicore, multicore, fiber-type disproportion,<br />

myotubular, c<strong>en</strong>tronuclear, nemaline)<br />

Limb-girdle muscular dystrophy<br />

Facioscapulohumeral muscular dystrophy<br />

359.1 03 Distrofia muscular (Becker) Muscular dystrophy (Becker)<br />

359.1 04 Distrofia muscular (Duch<strong>en</strong>ne) Muscular dystrophy (Duch<strong>en</strong>ne)<br />

359.1 05 Distrofia muscular congénita (Fukuyama,<br />

MCO, Walker-Warburg, <strong>de</strong>fici<strong>en</strong>te <strong>en</strong><br />

merosina o <strong>en</strong> integrina, miopatía <strong>de</strong><br />

Bethlem…)<br />

Cong<strong>en</strong>ital muscular dystrophy (Fukuyama,<br />

COMS, Walker-Warburg, merosine <strong>de</strong>fici<strong>en</strong>cy,<br />

integrin <strong>de</strong>fici<strong>en</strong>cy, Bethlem myopathy…)<br />

359.1 06 Emery-Dreifuss, <strong>en</strong>fermedad B<strong>en</strong>ign scapuloperoneal muscular dystrophy<br />

with early contractures (Emery-Dreifuss)<br />

359.2 01 Distrofia miotónica (Steinert) Dystrophia myotonica (Steinert)<br />

359.2 02 Miotonía congénita (Thoms<strong>en</strong>) Thoms<strong>en</strong>’s myotonia cong<strong>en</strong>ita<br />

359.2 03 Paramiotonía congénita (Eul<strong>en</strong>burg) Paramyotonia cong<strong>en</strong>ita of von Eul<strong>en</strong>burg<br />

359.2 04 Miotonía congénita (Becker) Cong<strong>en</strong>ital myotonia (Becker type)<br />

359.3 S/E Parálisis periódica familiar Periodic paralysis (familial)<br />

359.4 S/E Miopatía toxica o por fármacos Drug-induced myopathy<br />

359.5 S/E Miopatía <strong>en</strong> <strong>en</strong>fermedad <strong>en</strong>docrina Myopathy in <strong>en</strong>docrine diseases<br />

359.6 S/E Miopatía inflamatoria asociada a otras<br />

<strong>en</strong>fermeda<strong>de</strong>s<br />

Inflammatory myopathy associated with<br />

other disor<strong>de</strong>rs<br />

359.81 S/E Miopatía <strong>de</strong>l <strong>en</strong>fermo crítico Critical care myopathy<br />

359.89 01 Miopatía metabólica Myopathy in metabolic diseases

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