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Aplasia cutis congenita (also known as "Cutis aplasia," "Congenital absence of skin," and "Congenital scars) is the most common congenital
Kaynak: Aplasia cutis congenita

Radial aplasia is a congenital defect which affects the formation of the radius bone in the arm. The radius is the lateral bone which
Kaynak: Radial aplasia

Pure red cell aplasia (PRCA) or erythroblastopenia refers to a type of anemia affecting the precursors to red blood cells but not to
Kaynak: Pure red cell aplasia

Membranous aplasia cutis is a cutaneous condition, a type of aplasia cutis congenita , which can be seen along the embryonic fusion lines of
Kaynak: Membranous aplasia cutis

Microphthalmia–dermal aplasia–sclerocornea syndrome (also known as "MIDAS syndrome") is a condition characterized by linear skin lesions
Kaynak: Microphthalmia–dermal aplasia–sclerocornea syndrome

Leydig cell hypoplasia (or aplasia) (LCH), also known as Leydig cell agenesis, is a rare autosomal recessive genetic and endocrine
Kaynak: Leydig cell hypoplasia

Strong syndrome, congenital thymic aplasia, and thymic hypoplasia, is a syndrome caused by the deletion of a small piece of chromosome 22 .
Kaynak: DiGeorge syndrome

Atypical MRKH – Uterovaginal aplasia /hypoplasia with renal malformation or uterovaginal aplasia /hypoplasia with ovarian dysfunction
Kaynak: Müllerian agenesis

Symptoms may also include scoliosis and primary amenorrhea Synonyms include "Mullerian aplasia with hypoplastic thumbs", "Hypoplastic
Kaynak: Michels Caskey syndrome

As an example, chloramphenicol treatment is followed by aplasia in less than one in 40,000 treatment courses, and carbamazepine aplasia is
Kaynak: Aplastic anemia

always used precisely, it properly refers to an inadequate or below-normal number of cells Hypoplasia is similar to aplasia , but less severe.
Kaynak: Hypoplasia

Ulnar–mammary syndrome or Schinzel syndrome is a cutaneous condition characterized by nipple and breast hypoplasia or aplasia
Kaynak: Ulnar–mammary syndrome

This condition is also known as Brauer syndrome (hereditary symmetrical aplastic nevi of temples, bitemporal aplasia cutis congenita,
Kaynak: Focal facial dermal dysplasia

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