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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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

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amebiasis cutis

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amibiase cutanée

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atrophoderma [ atrophodermia | atrophia cutis ]

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atrophodermie