A rare multiple congenital anomalies syndrome with characteristics of mild intellectual disability, short stature, cardiac anomalies, mild dysmorphic features (macrocephaly, prominent forehead, hypertelorism, exophthalmos), cutis laxa, joint hyperlax

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syndrome cranio-facio-fronto-digital

SNOMEDCT-BE (macrocephaly, prominent forehead, hypertelorism, exophthalmos), cutis laxa, joint hyperlax / 763320005

SNOMEDCT-BE (disorder) / 763320005

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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

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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

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Others have searched : amyloidosis cutis dyschromia amyloidosis amyloidosis cutis amyloidosis of the liver amyloidosis of the skin cutie pie cutie pie meter cutie-pie survey meter cutis mamelonnata cutis mamelonnata pasini cutis marmorata cutis marmorata vascularis cutis verticis mamelonnata cutis verticis mamelonnata pasini hepatic amyloidosis liver amyloidosis senile cardiac amyloidosis

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'amyloidosis cutis'

Date index:2021-09-14 -

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Translation of "amyloidosis cutis " (English → French) :

Pour agences de traduction et traducteurs - For translation agencies & translators Paris - Brussels - Montreal - Genève - Luxembourg - Madrid Wordscope - Professional computer-assisted translation tools (CAT tools)

Pour agences de traduction et traducteurs - For translation agencies & translators

Paris - Brussels - Montreal - Genève - Luxembourg - Madrid

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