| HED | hereditary ectodermal dysplasia; hydrotropic electron-donor; hypohidrotic ectodermal dysplasia; unit... |
|---|---|
| APECED | Autoimmune Poly-Endocrinopathy Candidiasis Ectodermal Dystrophy |
| PNET | Primitive Neuro-Ectodermal(-Epithelial) Tumor |
| ACED | anhydrotic congenital ectodermal dysplasia |
| AEC | ankyloblepharon, ectodermal defects, and cleft lip [syndrome]; at earliest convenience; Atomic Energ... |
| AER | Apical Ectodermal Ridge |
|---|---|
| APECED | Autoimmune polyendocrinopathy candidiasis ectodermal dystrophy |
| ED | ectodermal dysplasia |
| HED | Hypohidrotic ectodermal dysplasia |
| A.E.D. | anhidrotic ectodermal dysplasia |
| ectodermal cloaca | The proctodeum of the embryo. (05 Mar 2000) |
|---|
| persistent cloaca | A condition in which the urorectal fold has failed to divide the cloaca of the embryo into rectal and urogenital portions. Synonym: sinus urogenitalis, urogenital sinus. (05 Mar 2000) |
|---|---|
| cloaca | 1. <zoology> A common passage for faecal, urinary and reproductive discharge in most lower vertebrates. 2. <embryology> The terminal end of the hindgut before division into rectum, bladder and genital primordia. 3. <pathology> An opening in the involucrum of a necrosed bone. (18 Nov 1997) |
| endodermal cloaca | Terminal portion of the hindgut internal to the cloacal membrane of the embryo. (05 Mar 2000) |
| exstrophy of the cloaca | A developmental anomaly in which an area of intestinal mucosa is interposed between two separate areas of the urinary bladder. Synonym: ectopia cloacae. (05 Mar 2000) |
| anhidrotic ectodermal dysplasia | A hereditary condition (most often x linked) that is characterised by the abnormal development of skin, absence of sweat glands, dry eyes and abnormal development of teeth. Symptoms include absent teeth, peg teeth, inability to sweat, thin skin and heat intolerance. Mucous membrane involvement may result in a foul-smelling nasal discharge. The inability to sweat leads to the inability to maintain normal body temperature in a warm environment. Some may exhibit fevers and will require artificial cooling. Inheritance: mostly sex-linked (X chromosome). Origin: Gr. Plassein = to form (12 Nov 1997) |
| apical ectodermal ridge | The layer of surface ectodermal cells at the apex of the embryonic limb bud; considered to exert an inductive influence on the condensation of underlying mesenchyme. (05 Mar 2000) |
| congenital ectodermal defect | Incomplete development of the epidermis and skin appendages; the skin is smooth and hairless, the facies abnormal, and the teeth and nails may be affected; sweating may be deficient. Synonym: congenital ectodermal dysplasia. (05 Mar 2000) |
| congenital ectodermal dysplasia | Incomplete development of the epidermis and skin appendages; the skin is smooth and hairless, the facies abnormal, and the teeth and nails may be affected; sweating may be deficient. Synonym: congenital ectodermal dysplasia. (05 Mar 2000) |
| hidrotic ectodermal dysplasia | Congenital dystrophy of the nails and hair with thickened nails and sparse or absent scalp hair; often associated with keratoderma of the palms and soles; teeth and sweat gland function are normal; autosomal dominant inheritance. (05 Mar 2000) |
| hypohidrotic ectodermal dysplasia | A hereditary condition (most often x linked) that is characterised by the abnormal development of skin, absence of sweat glands, dry eyes and abnormal development of teeth. Symptoms include absent teeth, peg teeth, inability to sweat, thin skin and heat intolerance. Mucous membrane involvement may result in a foul-smelling nasal discharge. The inability to sweat leads to the inability to maintain normal body temperature in a warm environment. Some may exhibit fevers and will require artificial cooling. Inheritance: mostly sex-linked (X chromosome). Origin: Gr. Plassein = to form (12 Nov 1997) |
| ectodermal | Relating to the ectoderm. Synonym: ectodermic. (05 Mar 2000) |
| ectodermal dysplasia | A hereditary condition (most often x linked) that is characterised by the abnormal development of skin, absence of sweat glands, dry eyes and abnormal development of teeth. Symptoms include absent teeth, peg teeth, inability to sweat, thin skin and heat intolerance. Mucous membrane involvement may result in a foul-smelling nasal discharge. The inability to sweat leads to the inability to maintain normal body temperature in a warm environment. Some may exhibit fevers and will require artificial cooling. Origin: Gr. Plassein = to form (27 Sep 1997) |
| ectrodactyly-ectodermal dysplasia-clefting syndrome | <syndrome> An autosomal recessive disorder resulting in defects of hands and feet; the ectodermal dysplasia causes fair skin, anodontia, and cleft palate. (05 Mar 2000) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|