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Malformatii congenitale, deformatii si anomalii cromozomiale

Malformatii congenitale, deformatii si anomalii cromozomiale

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<strong>Malformatii</strong> <strong>congenitale</strong>, <strong>deformatii</strong> <strong>si</strong> <strong>anomalii</strong> <strong>cromozomiale</strong><br />

Q86.84 <strong>Malformatii</strong> <strong>congenitale</strong> datorite<br />

agentilor citotoxici<br />

Q86.85 <strong>Malformatii</strong> <strong>congenitale</strong> datorite altor<br />

medicamente<br />

Exclude: dismorfism datorit warfarinei<br />

(Q86.2)<br />

Q86.86 <strong>Malformatii</strong> <strong>congenitale</strong> datorite<br />

radiatiilor ionizante<br />

Q86.87 <strong>Malformatii</strong> <strong>congenitale</strong> datorite<br />

metililor mercurului<br />

Q86.89 <strong>Malformatii</strong> <strong>congenitale</strong> datorite<br />

cauzelor exogene specificate<br />

Q87 Alte <strong>si</strong>ndroame de malformatii<br />

<strong>congenitale</strong> specificate afectand<br />

<strong>si</strong>steme multiple<br />

Q87.0 Sindroame de malformatii <strong>congenitale</strong><br />

afectand in special fizionomia fetei<br />

Q87.01 Acrocefalopoli<strong>si</strong>ndactilia<br />

Acrocefalopoli<strong>si</strong>ndactilia tip I, <strong>si</strong>ndromul<br />

Noack<br />

Acrocefalopoli<strong>si</strong>ndactilia tip II,<br />

<strong>si</strong>ndromul Carpenter<br />

Q87.02 Acrocefalo<strong>si</strong>ndactilia<br />

Sindromul Apert<br />

Cefalodactilia Vogt<br />

Q87.03 Sindromul criptoftalmic<br />

Sindromul Fraser<br />

Q87.04 Sindromul Treacher Collins<br />

[-Franceschetti] [-Klein]<br />

Exclude: disostoza mandibulo-faciala<br />

producandu-se ca o<br />

anomalie izolata (Q75.4)<br />

Q87.05 Sindromul Hallerman-Streiff<br />

Exclude: disostoza oculo-mandibulara<br />

producandu-se ca o<br />

anomalie izolata (Q75.5)<br />

Q87.06 Episodul Pierre Robin<br />

Sindromul <strong>si</strong> episodul Robin<br />

Q87.07 Sindromul Pena-Shokeir<br />

Sindromul hipoplaziei pulmonare cu<br />

<strong>anomalii</strong> faciale anchilozante<br />

camptodactile<br />

368<br />

Q87.09 Alte <strong>si</strong>ndroame de malformatii<br />

<strong>congenitale</strong> afectand in special<br />

fizionomia fetei<br />

Sindrom de malformatii <strong>congenitale</strong><br />

afectand in special fizionomia fetei NOS<br />

Ciclopia [ciclop][ciclopism][<strong>si</strong>noftalmia]<br />

Discraniopigofalangism<br />

Artro-oftalmia progre<strong>si</strong>va ereditara<br />

Sindrom:<br />

- Goldenhar<br />

- Moebius<br />

- Mohr<br />

- oculo-auriculo-vertebral [microzomia<br />

hemifaciala]<br />

- orofacial-digital tip I <strong>si</strong> I<br />

- Stickler<br />

- trico-rino-falangian tip I <strong>si</strong> II [Langer-<br />

Giedion]<br />

- Ullrich-Feichtiger<br />

- fizionomia Whistling<br />

Exclude: cherubism (K10.8)<br />

<strong>si</strong>ndromul Waardenburg<br />

(E70.3)<br />

Q87.1 Sindroame de malformatii <strong>congenitale</strong><br />

asociate in special cu statura scurta<br />

Exclude: <strong>si</strong>ndromul Ellis-van Creveld<br />

(Q77.6)<br />

<strong>si</strong>ndromul Turner(-Ullrich)<br />

(Q96.-)<br />

Q87.11 Sindromul Cockayne<br />

Q87.12 Sindromul Cornelia de Lange<br />

Pitic Amsterdam [<strong>si</strong>ndromul Brachmannde<br />

Lange]<br />

Q87.13 Sindromul Noonan<br />

Afectiune asemanatoare <strong>si</strong>ndromului<br />

Turner<br />

Q87.14 Sindromul Prader-Willi<br />

Q87.15 Sindromul Russell-Silver<br />

Q87.16 Sindromul Seckel<br />

Nanism cu cap de pasare<br />

Nanism primordial microcefalic<br />

Q87.17 Sindromul Smith-Lemli-Opitz<br />

Deficienta de 7-dehidrocolesterol<br />

reductaza<br />

Q87.18 Sindromul Sjogren-Larsson<br />

Alcoolism grasos: deficienta in<br />

nicotinamide adenine dinucleotide<br />

oxidoreductaza<br />

Lista Tabelară a Bolilor ICD-10-AM 2002

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