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Aplasia cutis congenita
Aplasia cutis with myopia syndrome
Autosomal recessive cutis laxa type 2B
Cutis aplasia
Type 2 aplasia cutis

Translation of "Type 2 aplasia cutis " (English → French) :

TERMINOLOGY
see also In-Context Translations below
Type 2 aplasia cutis
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syndrome d'Adams-Oliver
SNOMEDCT-BE (disorder) / 34748004
SNOMEDCT-BE (disorder) / 34748004
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https://browser.ihtsdotools.or (...) [HTML]
An extremely rare association syndrome, described in only two brothers to date (one of which died at 2 months of age), characterized by aplasia cutis congenita of the vertex and generalized edema (as well as hypoproteinemia and lymphopenia) due to in
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aplasie cutanée congénitale autosomique récessive
SNOMEDCT-BE (one of which died at 2 months of age), characterised by aplasia cutis congenita of the vertex and generalised oedema (as well as hypoproteinaemia and lymphopenia) due to / 720500008
SNOMEDCT-BE (disorder) / 720500008
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
An extremely rare association syndrome, described in only two brothers to date (one of which died at 2 months of age), characterised by aplasia cutis congenita of the vertex and generalised oedema (as well as hypoproteinaemia and lymphopenia) due to
https://browser.ihtsdotools.or (...) (...) [HTML]
syndrome d'aplasie cutanée congénitale-lymphangiectasie intestinale
SNOMEDCT-BE (one of which died at 2 months of age), characterised by aplasia cutis congenita of the vertex and generalised oedema (as well as hypoproteinaemia and lymphopenia) due to / 720500008
SNOMEDCT-BE (disorder) / 720500008
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
Aplasia cutis with myopia syndrome
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syndrome d'aplasie cutanée-myopie
SNOMEDCT-BE (disorder) / 720499004
SNOMEDCT-BE (disorder) / 720499004
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
Aplasia cutis congenita, nevus sebaceous syndrome
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syndrome d'aplasie cutanée congénitale-naevus sébacé
SNOMEDCT-BE (disorder) / 774209001
SNOMEDCT-BE (disorder) / 774209001
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
Aplasia cutis congenita
https://icd.who.int/browse10/2 (...) (...) [HTML]
Aplasie ectodermique congénitale
WORLD HEALTH ORGANIZATION ICD-10: Q84.8
WORLD HEALTH ORGANIZATION ICD-10: Q84.8
https://icd.who.int/browse10/2 (...) (...) [HTML]
https://icd.who.int/browse10/2 (...) [HTML]
Cutis aplasia
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aplasia cutis congenita
SNOMEDCT-BE (disorder) / 35484002
SNOMEDCT-BE (disorder) / 35484002
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
Autosomal recessive cutis laxa type 2B
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cutis laxa autosomique récessive type 2B
SNOMEDCT-BE (disorder) / 778068007
SNOMEDCT-BE (disorder) / 778068007
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https://browser.ihtsdotools.or (...) [HTML]
IN-CONTEXT TRANSLATIONS
Uncommon side effects (may affect up to 1 in 100 people) A type of anaemia called pure red cell aplasia Loss of sense of taste Symptoms of heart failure such as breathlessness, difficulty breathing when lying down, swelling of the feet or legs Blockage or obstruction of a blood vessel (vein) in the leg (deep vein thrombosis).
http://www.ema.europa.eu/docs/ (...) (...) [HTML]
- Blocage ou obstruction d’un vaisseau sanguin (veine) dans la jambe (thrombose veineuse profonde).
http://www.ema.europa.eu/docs/ (...) (...) [HTML]
http://www.ema.europa.eu/docs/ (...) [HTML]


Others have searched : aplasia cutis congenita    aplasia cutis with myopia syndrome    cutis aplasia    type 2 aplasia cutis    Type 2 aplasia cutis    


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'Type 2 aplasia cutis'

Date index:2023-07-22 -

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