Vertaling van "thyreo-aplasia " (Nederlands → Engels) :

athyrea | athyria | athyrie | thyreo-aplasia | thyreo-aplasia congenita
congenital athyreosis | congenital athyria

anemie van Fanconi | familiale hypoplastische anemie | pancytopenie met misvormingen | '(Pure) red cell aplasia' | congenitaal | '(Pure) red cell aplasia' | van kinderen | '(Pure) red cell aplasia' | primair | syndroom van Blackfan-Diamond
Aplasia, (pure) red cell (of):congenital | infants | primary | Blackfan-Diamond syndrome Familial hypoplastic anaemia Fanconi's anaemia Pancytopenia with malformations

aplasia moniliformis | aplasia pilorum intermittens | monilethrix | parelsnoerhaar | pilus moniliformis | rozenkranshaar
monilethrix

aplasia vesicae
aplasia of urinary bladder

verworven 'pure red cell aplasia' [erytroblastopenie]
Acquired pure red cell aplasia [erythroblastopenia]

chronische verworven 'pure red cell aplasia'
Chronic acquired pure red cell aplasia

aplasia cutis congenita, naevus sebaceus-syndroom
Aplasia cutis congenita, nevus sebaceous syndrome

aplasia cutis, myopiesyndroom
Aplasia cutis with myopia syndrome

autosomaal recessieve aplasia cutis
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