| CDF | chondrodystrophia foetalis |
|---|---|
| ASD | aldosterone secretion defect; Alzheimer senile dementia; antisiphon device; arthritis syphilitica de... |
| DMD | disease-modifying drug; Doctor of Dental Medicine; Duchenne muscular dystrophy; dystonia musculorum ... |
| rachitis foetalis | congenital rickets |
|---|---|
| rachitis foetalis annularis | Congenital enlargement of the epiphyses of the long bones. (05 Mar 2000) |
| rachitis foetalis micromelica | A congenital condition in which development of the long bones is deficient. (05 Mar 2000) |
| pars foetalis placentae | <embryology> Placenta foetalis, the chorionic portion of the placenta, containing the foetal blood vessels, from which the funis develops; specifically, in humans, it develops from the chorion frondosum. Synonym: pars foetalis placentae. (05 Mar 2000) |
| chondromalacia foetalis | An intrauterine form of chondromalacia in which the foetus is born dead with soft pliable limbs. (05 Mar 2000) |
| hydrops foetalis | <embryology, paediatrics> A severe form of the genetic disorder thalassaemia in which all four alpha chain polypeptides making up the haemoglobin molecule (the protein which transports oxygen in the body) are missing due to a defect in the gene which codes for them. As a result, affected individuals die at or before birth. (09 Oct 1997) |
| ichthyosis foetalis | Recessive condition in Holstein and Norwegian red poll cattle resembling harlequin foetus in humans. See: harlequin foetus (05 Mar 2000) |
| erythroblastosis foetalis | <haematology> A condition which develops in the foetus due to an incompatibility between the mother's blood type (RH factor) and the baby's. Maternal antibodies, which enter the foetal circulation during delivery attack the baby's red blood cells leading to haemolysis (rupture of the cells). Symptoms include an infant with an enlarged liver and spleen, swelling, jaundice and anaemia. (27 Sep 1997) |
| keratosis diffusa foetalis | most common form of ichthyosis characterised by prominent scaling especially on the exterior surfaces of the extremities. It is inherited as an autosomal dominant trait. (12 Dec 1998) |
| arthritis deformans | A systemic disease, seen more commonly in women which affects connective tissue, particularly the synovial tissue within joints. Arthritis is the main clinical feature and involves many joints in the body, especially those of the hand and feet. In this disease, there is thickening of the soft tissues around the joints and extension of the synovial tissue over articular cartilage (which becomes eroded). A chronic and progressive course is common with joint deformities and disability. Juvenile rheumatoid arthritis is a variant which affects children. (27 Sep 1997) |
| peritonitis deformans | A chronic peritonitis in which thickening of the membrane and contracting adhesions cause shortening of the mesentery and kinking and retraction of the intestines. (05 Mar 2000) |
| hyperostosis corticalis deformans | Marked irregular thickening of the skull and bone cortex, with thickening and widening of the shafts of long bones and high serum alkaline phosphatase; autosomal recessive inheritance. (05 Mar 2000) |
| spondylitis deformans | Arthritis and osteitis deformans involving the spinal column; marked by nodular deposits at the edges of the intervertebral disks with ossification of the ligaments and bony ankylosis of the intervertebral articulations, it results in a rounded kyphosis with rigidity. Synonym: Bechterew's disease, poker back, Strumpell's disease. (05 Mar 2000) |
| dystonia musculorum deformans | A genetic, environmental, or idiopathic disorder, usually beginning in childhood or adolescence, marked by muscular contractions that distort the spine, limbs, hips, and sometimes the cranial-innervated muscles. The abnormal movements are increased by excitement and, at least initially, abolished by sleep. The musculature is hypertonic when in action, hypotonic when at rest. Hereditary forms usually begin with involuntary posturing of the foot or hand (autosomal recessive form ) or of the neck or trunk (autosomal dominant form ); both forms may progress to produce contortions of the entire body. Synonym: progressive torsion spasm, torsion disease of childhood, torsion dystonia, Ziehen-Oppenheim disease. (05 Mar 2000) |
| osteitis deformans | This is a disease of bone that initially results in the excessive resorption of bone (by osteoclasts) followed by the replacement of normal bone marrow with vascular and fibrous tissue. Many patients are asymptomatic and diagnosed by routine X-rays. (27 Sep 1997) |
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