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Symptoms » Knock-knee » Glossary
 

Glossary for Knock-knee

Medical terms related to Knock-knee or mentioned in this section include:

  • 49,XXXXY syndrome: A rare sex chromosome abnormality where there are three extra copies of the X chromosome.
  • Arm symptoms: Symptoms affecting the arm
  • Bone symptoms: Symptoms affecting the body's bones
  • Camurati-Engelmann Disease: A very rare genetic disease thickening of areas of bone causing pain, weakness and wasting. Usually affects the legs during childhood. Also called diaphyseal dysplasia.
  • Cat Eye Syndrome: A rare chromosomal disorder involving abnormalities of chromosome 22 and characterized by coloboma of the iris, down-slanting palpebral fissures and anal atresia.
  • Cohen Syndrome: A rare genetic disorder characterized by reduced muscle tone, obesity and prominent front teeth.
  • Dyggve-Melchior-Clausen Syndrome: A rare genetic bone growth disorder characterized by short stature and other skeletal deformities.
  • Face symptoms: Symptoms affecting the face
  • Fairbank disease: A rare inherited disorder that affects the secondary growth centers of bones usually in the hips, knees and ankles and results in mild dwarfism.
  • Homocystinuria syndrome: A rare genetic connective tissue disorder caused by an enzyme deficiency and characterized by dislocation of eye lens, malar flush and osteoporosis.
  • Hypomelanosis of Ito: A rare genetic neurocutaneous disorder characterized by unusual patterns of depigmented skin and associated disorders such as seizures, psychomotor retardation and eye abnormalities.
  • Joint symptoms: Symptoms affecting the joints.
  • Knee conditions: Any condition that affects the knee
  • Knee pain: Pain in or around the knee joint
  • Knee symptoms: Symptoms affecting the knee
  • Leg symptoms: Symptoms affecting the leg
  • Limb symptoms: Symptoms affecting the limbs
  • Marinesco-Sjogren I: A rare condition characterized by cerebellar ataxia, speaking difficulty, mental retardation, short stature and tooth, hair and nail abnormalities.
  • Melnick-Needles syndrome: A rare genetic bone disorder characterized by skeletal abnormalities and characteristic facial abnormalities.
  • Metaphyseal dysplasia Pyle type: A rare genetic disorder characterized by bone deformities involving the limbs, skull and other parts of the skeleton.
  • Morquio syndrome type A: A rare inherited biochemical disorder characterized by the accumulation of mucopolysaccharides (glycosaminoglycans) in various body tissues due to insufficient amounts of the enzyme (galactosamine-?-sulfate) needed to break it down.
  • Morquio syndrome, type B: A rare inherited biochemical disorder characterized by the accumulation of mucopolysaccharides (glycosaminoglycans) in various body tissues due to insufficient amounts of the enzyme (? galactosidase) needed to break it down.
  • Mucopolysaccharidosis type 6: A rare inherited biochemical disorder characterized by the accumulation of mucopolysaccharides (glycosaminoglycans) in various body tissues due to insufficient amounts of the enzyme (Arylsulfatase ?) needed to break it down.
  • Musculoskeletal symptoms: Symptoms affecting muscles or bones of the skeleton.
  • Nievergelt syndrome: A rare inherited bone disease which causes abnormalities in the lower leg and lower arm bones as well as dwarfism and digit anomalies.
  • Nonkeratan-sulfate-excreting Morquio syndrome: A rare inherited biochemical disorder characterized by the accumulation of mucopolysaccharides (glycosaminoglycans) in various body tissues due to insufficient amounts of certain enzymes needed to break it down. This disorder is distinguished form other similar conditions by the fact that no keratosulfate is excreted in the urine.
  • Pyle disease: A rare genetic disorder characterized by numerous bone abnormalities as well as loss of vision and hearing.
  • Skeletal symptoms: Symptoms affecting the skeletal system such as the bones.
  • Spondyloenchondrodysplasia: A rare genetic disorder where abnormal bone development resluts in symptoms such as flattened spine bones, short stature, large joints and other anomalies. The disorder is also characterized by the development of benign cartilage growths in bones which affects it's growth and strength.
  • Spondyloepimetaphyseal dysplasia, hypotrichosis: An inherited bone growth disorder characterized by short stature, bone abnormalities and vision problems. An additional feature of this condition is the reduced amount of hair (hypotrichosis). The bone abnormalities are due to a genetic mutation that affects the development of bone and connective tissue.
  • Strudwick syndrome: An inherited bone growth disorder characterized by short stature, bone abnormalities and vision problems. The bone abnormalities are due to a genetic mutation that affects the development of bone and connective tissue.
  • Summitt syndrome: A very rare genetic disorder abnormalities of the head, hands and feet as well as obesity.

Conditions listing medical symptoms: Knock-knee:

The following list of conditions have 'Knock-knee' or similar listed as a symptom in our database. This computer-generated list may be inaccurate or incomplete. Always seek prompt professional medical advice about the cause of any symptom.

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