| FOP | fibrodysplasia ossificans progressiva; forensic pathology |
|---|---|
| POG | pediatric oncology group; polymyositis ossificans generalisata |
| POP | diphosphate group; pain on palpation; paroxypropione; persistent occipitoposterior [fetal position];... |
| POT | periostitis ossificans toxica; postoperative treatment |
| ACC | accommodation; acetyl coenzyme A carboxylase; acinic cell carcinoma; acute care center; adenoid cyst... |
| FOP | Fibrodysplasia ossificans progressiva |
|---|---|
| AHC | Adrenal hypoplasia congenita |
| ACC | Aplasia cutis congenita |
| AMC | Arthrogryposis Multiplex Congenita |
| CMTC | Cutis Marmorata Telangiectatica Congenita |
| fibrodysplasia | Abnormal development of fibrous connective tissue. Fibrodysplasia ossificans progressiva, a generalised disorder of connective tissue in which bone replaces tendons, fasciae, and ligaments; a lethal genetic disorder inferred from indirect evidence to have autosomal dominant inheritance. See: fibrous dysplasia of bone. (05 Mar 2000) |
|---|---|
| pelvospondylitis ossificans | Deposit of bony substance between the vertebrae of the sacrum. Origin: L. Pelvis, basin, + G. Spondylos, vertebra, + -itis; L. Os, bone, + facio, to make (05 Mar 2000) |
| myositis ossificans | A disease characterised by bony deposits or the ossification of muscle tissue. (12 Dec 1998) |
| myositis ossificans circumscripta | Local deposit of bone in a muscle, usually following prolonged trauma; e.g., riders' bone. (05 Mar 2000) |
| myositis ossificans progressiva | <radiology> Progressive skeletal fusion, ossification of ligaments, nuchal ligament, pelvic entheses, asymptomatic at birth, 90% have short great toes (12 Dec 1998) |
| lipoma ossificans | A lipoma in which metaplasia occurs and small foci of bone are formed. (05 Mar 2000) |
| amaurosis congenita of Leber | An autosomal recessive cone-rod abiotrophy causing blindness or severely reduced vision at birth. (05 Mar 2000) |
| amyoplasia congenita | Limitation of range of joint motion and contractures present at birth, usually involving multiple joints; a syndrome probably of diverse aetiology that may result from changes in spinal cord, muscle, or connective tissue. Several forms exist, autosomal dominant, recessive, and X-linked. Synonym: amyoplasia congenita. (05 Mar 2000) |
| amyotonia congenita | Atonic pseudoparalysis of congenital origin (neither familial nor hereditary), observed especially in infants and characterised by absences of muscular tone only in muscles innervated by the spinal nerves. Synonym: congenital atonic pseudoparalysis, myatonia congenita, Oppenheim's disease, Oppenheim's syndrome. An indefinite term for a number of congenital neuromuscular disorders that cause generalised myotonia in young children, and that have a benign course (static or regressive). (05 Mar 2000) |
| aplasia cutis congenita | Congenital absence or deficiency of a localised area of skin, with the base of the defect covered by a thin translucent membrane; most often a single area near the vertex of the scalp, but may occur in other areas; underlying structures may also be affected; autosomal inheritance, either dominant or recessive. (05 Mar 2000) |
| arthrogryposis multiplex congenita | Limitation of range of joint motion and contractures present at birth, usually involving multiple joints; a syndrome probably of diverse aetiology that may result from changes in spinal cord, muscle, or connective tissue. Several forms exist, autosomal dominant, recessive, and X-linked. Synonym: amyoplasia congenita. (05 Mar 2000) |
| pachyonychia congenita | A syndrome of ectodermal dysplasia of abnormal thickness and elevation of nail plates with palmar and plantar hyperkeratosis; the tongue is whitish and glazed owing to papillary atrophy; autosomal dominant inheritance. Synonym: Jadassohn-Lewandowski syndrome. (05 Mar 2000) |
| chondrodystrophia calcificans congenita | A developmental error of the epiphyses characterised by severe deformities, epiphyses ossified from several discrete centres and with a stippled appearance, and thickened shafts of the long bones; congenital cataract and mental retardation are often present. There is an autosomal dominant form and an autosomal recessive form. Synonym: chondrodysplasia punctata, chondrodystrophia calcificans congenita, hypoplastic foetal chondrodystrophy, stippled epiphysis. (05 Mar 2000) |
| chondrodystrophia congenita punctata | Congenital shortening of the humerus and femur, with stippled epiphyses, high-arched palate, cataracts, erythroderma in the newborn, and scaling followed by follicular atrophoderma; there is also an autosomal dominant inheritance pattern . Synonym: chondrodystrophia congenita punctata. (05 Mar 2000) |
| myatonia congenita | Atonic pseudoparalysis of congenital origin (neither familial nor hereditary), observed especially in infants and characterised by absences of muscular tone only in muscles innervated by the spinal nerves. Synonym: congenital atonic pseudoparalysis, myatonia congenita, Oppenheim's disease, Oppenheim's syndrome. An indefinite term for a number of congenital neuromuscular disorders that cause generalised myotonia in young children, and that have a benign course (static or regressive). (05 Mar 2000) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|