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Aplasia (/əˈpleɪʒə/ ; from Gr**** a, "not", "no" + plasis, "formation") is a
birth defect where an
organ or
tissue is
wholly or
largely absent. It is caused...
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Michel aplasia, also
known as
complete labyrinthine aplasia (CLA), is a
congenital abnormality of the
inner ear. It is
characterized by the
bilateral absence...
- Pure red cell
aplasia (PRCA) or
erythroblastopenia refers to a type of
aplastic anemia affecting the
precursors to red
blood cells but
usually not to...
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Aplasia cutis congenita is a rare
disorder characterized by
congenital absence of skin.
Ilona J.
Frieden classified ACC in 1986 into 9
groups on the basis...
- Müllerian agenesis, also
known as Müllerian
aplasia, ****l agenesis, or Mayer–Rokitansky–Küster–Hauser
syndrome (MRKH syndrome), is a
congenital malformation...
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Radial aplasia is a
congenital defect which affects the
formation of the
radius bone in the arm. The
radius is the
lateral bone (thumb side)
which connects...
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Aplasia cutis-myopia
syndrome is a rare
genetic disorder characterized by a
combination of
aplasia cutis congenita, high myopia, and
dysfunction of the...
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Chloramphenicol treatment is ****ociated with
aplasia in less than one in 40,000
treatment courses, and
carbamazepine aplasia is even rarer.
Exposure to ionizing...
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Aplasia cutis congenita-intestinal
lymphangiectasia syndrome is a very rare
genetic disorder which is
characterized by
aplasia cutis congenita, intestinal...
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Fibular aplasia-ectrodactyly
syndrome (or
other synonyms such as brachydactyly-ectrodactyly with
fibular aplasia or hypoplasia) is a very rare genetic...
