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

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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

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Vitamin A deficiency with conjunctival xerosis

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Avitaminose A avec xérosis conjonctival

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https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]

Vitamin A deficiency with Bitot's spot and conjunctival xerosis

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Avitaminose A avec taches de Bitot et xérosis conjonctival

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https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]

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Date index: 2023-05-01