syndrome d'aplasie cutanée congénitale-lymphangiectasie intestinale
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
SNOMEDCT-BE (disorder) / 720500008
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
