| ASLN | Alport syndrome-like hereditary nephritis |
|---|---|
| HACR | hereditary adenomatosis of the colon and rectum |
| HAE | health appraisal examination; hearing aid evaluation; hepatic artery embolism; hereditary angioneuro... |
| HANE | hereditary angioneurotic edema |
| HBC | hereditary breast cancer |
| retinal dysplasia | <ophthalmology> Congenital, often bilateral, retinal abnormality characterised by the arrangement of outer nuclear retinal cells in a palisading or radiating pattern surrounding a central ocular space. This disorder is sometimes hereditary. (12 Dec 1998) |
|---|---|
| cervical dysplasia | A term which describes precancerous changes to the epithelial cells lining the cervix. The diagnosis is made from the microscopic examination of a PAP smear acquired tissue specimen. Less than 5% of all PAP smears will show cervical dysplasia. The peak incidence is in women 25 to 35 years of age. Risk factors include multiple sexual partners, early onset of sexual activity (less than 18), early childbearing (less than 16) and past medical history of a sexually transmitted disease (for example genital warts, genital herpes, HIV infection). Treatment is based on the degree of dysplasia present, as judged by a pathologist. Treatments include cryotherapy and conisation. Origin: Gr. Plassein = to form (27 Sep 1997) |
| cervix dysplasia | A spectrum of histologic changes in the epithelium of the cervix uteri which may begin as a superficial lesion and progress to invasive carcinoma. (12 Dec 1998) |
| periapical cemental dysplasia | <dentistry> A benign, painless, non-neoplastic condition of the jaws which occurs almost exclusively in middle-aged black females. The lesions are usually multiple, most frequently involve vital mandibular anterior teeth, surround the root apices, and are initially radiolucent (becoming more opaque as they mature). Synonym: periapical osteofibrosis. (21 Jun 2000) |
| metaphyseal dysplasia | <radiology> (Pyle disease) also known as: craniometaphyseal dysplasia, autosomal recessive, failure of modeling of cylindrical bones, Erlenmeyer flask appearance of metaepiphyses (12 Dec 1998) |
| metaphysial dysplasia | An abnormality that occurs when new bone at the metaphyses of long bones fails to undergo remodeling to the normal tubular structure; the ends of long bones appear to be expanded and porotic, with thin cortex; there may be an associated overgrowth of cranial bones (craniometaphysial dysplasia). (05 Mar 2000) |
| chondroectodermal dysplasia | Triad of chondrodysplasia, ectodermal dysplasia, and polydactyly, with congenital heart defects in over half of patients; autosomal recessive inheritance. Synonym: Ellis-van Creveld syndrome. (05 Mar 2000) |
| cleidocranial dysplasia | <paediatrics> An inherited disorder of bone development transmitted with an autosomal dominant pattern. Characteristics include absent or incompletely formed collar bones, dental abnormalities, joint laxity and a characteristic facial appearance (heavy brow, protruding jaw, wide nasal bridge and malaligned teeth). Inheritance: autosomal dominant. Origin: Gr. Plassein = to form (27 Sep 1997) |
| Mondini dysplasia | Congenital anomaly of osseus and membranous labyrinth characterised by aplastic cochlea, and deformity of the vestibule and saemicircular canals with partial or complete loss of auditory and vestibular function; may be associated with spontaneous cerebrospinal fluid otorrhoea resulting in meningitis. See: Mondini deafness. (05 Mar 2000) |
| monostotic fibrous dysplasia | Fibrous dysplasia of a single bone. Synonym: localised osteitis fibrosa, osteitis fibrosa circumscripta. (05 Mar 2000) |
| mucoepithelial dysplasia | An epithelial cell dishesive disease characterised by red, periorificial mucosal lesions of oral, nasal, vaginal, urethral, anal, bladder, and conjunctival mucosa, with cataracts, follicular keratosis, non-scarring alopecia, frequent pulmonary infections, pneumothorax, and sometimes cor pulmonale; autosomal dominant inheritance. (05 Mar 2000) |
| congenital dysplasia of the hip | A malformation of the hip joint that is present at birth. Genetic factors likely play a role in this disorder. Features include hip dislocation, asymmetry of leg positions, asymmetric fat folds and diminished movement on the affected side. Some children will exhibit little or no features and must be diagnosed by physical examination of the hip joints. (27 Sep 1997) |
| congenital hip dysplasia | A malformation of the hip joint that is present at birth. Genetic factors likely play a role in this disorder. Features include hip dislocation, asymmetry of leg positions, asymmetric fat folds and diminished movement on the affected side. Some children will exhibit little or no features and must be diagnosed by physical examination of the hip joints. Origin: Gr. Plassein = to form (27 Sep 1997) |
| multiple epiphysial dysplasia | A dominantly inherited abnormality of epiphyses characterised by difficulty in walking, pain and stiffness of joints, stubby fingers, and often dwarfism of short-limb type; on X-ray examination, the epiphyses are mottled and irregular; ossification centres are late in appearance and may be multiple, but the vertebrae are normal. There is also an autosomal recessive form . Synonym: dysplasia epiphysialis multiplex. (05 Mar 2000) |
| cortical dysplasia | A malformative disorganization of the cytoarchitecture of the cortex relative to neurons. (05 Mar 2000) |