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Symptoms » Foot deformities » Glossary
 

Glossary for Foot deformities

Medical terms related to Foot deformities or mentioned in this section include:

  • Amitriptyline -- Teratogenic Agent: There is strong evidence to indicate that exposure to Amitriptyline during pregnancy may have a teratogenic effect on the fetus. A teratogen is a substance that can cause birth defects. The likelihood and severity of defects may be affected by the level of exposure and the stage of pregnancy that the exposure occurred at.
  • Amnion rupture sequence: A rare disorder where the amniotic sac is ruptured resulting in various abnormalities.
  • Arm symptoms: Symptoms affecting the arm
  • Arthrogryposis: A condition which is characterized by the persistent flexure of a joint
  • Bilateral Renal Agenesis: Failure of both kidneys to from during embryogenesis.
  • Camptomelic dysplasia I: A rare condition characterized by dwarfism due to bowed shin and thigh bones.
  • Camptomelic dysplasia II: A rare condition characterized by dwarfism due to bowed shin and thigh bones which tend to be shorter and wider than normal.
  • Charcot-Marie-Tooth disease deafness recessive type: CMT is an inherited neurological disease characterized by the gradual degeneration of nerves which starts in the hands and feet and results in progressive numbness, muscle weakness and loss of function. Type 4D is inherited recessively and is caused by a defected in a gene in chromosome 8 and is a severe form of the disease that also involves deafness.
  • Charcot-Marie-Tooth disease, Type 2AI: CMT is an inherited neurological disease characterized by the gradual degeneration of nerves which starts in the hands and feet and results in progressive numbness, muscle weakness and loss of function. Type 2A1 has an autosomal dominant inheritance and involves a defect in the KIF1B gene on chromosome 1p36.
  • Charcot-Marie-Tooth disease, Type 2AII: CMT is an inherited neurological disease characterized by the gradual degeneration of nerves which starts in the hands and feet and results in progressive numbness, muscle weakness and loss of function. Type 2A2 has an autosomal dominant inheritance and involves a defect in the MFN2 gene on chromosome 1p36.
  • Congenital fiber type disproportion: A rare inherited disease involving abnormalities in the growth of type I muscle fibers.
  • Deformity symptoms: Various types of deformity
  • Ehlers danlos syndrome: An inherited disorder of the connective tissue causing it to become weak and fragile. Connective tissue is found in skin, muscles, tendons and ligaments and hence all of these may be affected by weakness
  • Face symptoms: Symptoms affecting the face
  • Foot conditions: Any condition that may affect the foot
  • Foot deformity: A alteration of the foot structurally that it doesn't appear as normal
  • Foot pain: Pain affecting one or both feet
  • Foot symptoms: Symptoms affecting one or both feet
  • Friedreich's ataxia: Progressive muscle weakness from nerve damage.
  • Frints -- De Smet -- Fabry -- Fryns syndrome: A rare syndrome characterized by a variation of Larsen syndrome where the physical manifestations are asymmetrical. This is believed to be a mosaic form of the genetic condition where the genetic anomaly is present in only some of the body's cells leading to asymmetric manifestations.
  • Game-Friedman-Paradice syndrome: A rare condition characterized by retarded growth, hydrocephaly, underdeveloped lungs and various other anomalies. The condition was observed in four offspring from one family.
  • Gout: Painful joints, most commonly the big toe.
  • Head symptoms: Symptoms affecting the head or brain
  • High arched foot: High arch between the toes and the heel.
  • Hypopigmented lesions in children: Hypopigmented lesions in children refers are sores or ulcers that are colorless or have lost color in a child.
  • Injury: Any damage inflicted in the body
  • Kabuki syndrome: A rare genetic disorder characterized by distinctive facial features.
  • Leg symptoms: Symptoms affecting the leg
  • Leprosy, susceptibility to, 1: A chronic, progressive infectious disease caused by Mycobacterium leprae which causes skin sores and also affects the eyes, mucous membranes and peripheral nerves. The range of manifestations and severity of symptoms is quite variable. Researchers have discovered a number of genetic mutations linked to an increased susceptibility to leprosy. Type 1 is linked to a defect on chromosome 10p13.
  • Leprosy, susceptibility to, 2: A chronic, progressive infectious disease caused by Mycobacterium leprae which causes skin sores and also affects the eyes, mucous membranes and peripheral nerves. The range of manifestations and severity of symptoms is quite variable. Researchers have discovered a number of genetic mutations linked to an increased susceptibility to leprosy. Type 2 is linked to a defect on chromosome 6q25.2-q27.
  • Leprosy, susceptibility to, 3: A chronic, progressive infectious disease caused by Mycobacterium leprae which causes skin sores and also affects the eyes, mucous membranes and peripheral nerves. The range of manifestations and severity of symptoms is quite variable. Researchers have discovered a number of genetic mutations linked to an increased susceptibility to leprosy. Type 3 is linked to a defect on chromosome 4q32 and 4p14.
  • Leprosy, susceptibility to, 4: A chronic, progressive infectious disease caused by Mycobacterium leprae which causes skin sores and also affects the eyes, mucous membranes and peripheral nerves. The range of manifestations and severity of symptoms is quite variable. Researchers have discovered a number of genetic mutations linked to an increased susceptibility to leprosy. Type 4 is linked to a defect on chromosome 6p21.3.
  • Limb symptoms: Symptoms affecting the limbs
  • Lower leg symptoms: Symptoms affecting the lower legs, calves and shins.
  • Macroepiphyseal dysplasia with osteoporosis, wrinkled skin, and aged appearance: A rare disorder characterized by osteoporosis, wrinkled skin, aged appearance and abnormal bone development.
  • Maffucci Syndrome: A rare genetic disorder characterized by benign cartilage overgrowths, skeletal deformities and dark red irregular skin patches.
  • Meckel Syndrome: A rare genetic disorder involving numerous abnormalities and characterized by death within the first few weeks.
  • Movement symptoms: Changes to movement or motor abilities
  • Myopathy, congenital fiber-type disproportion: A rare inherited disease involving abnormalities in the growth of type I muscle fibers.
  • Neural tube defect: Any defect that occurs to the neural tube
  • Neuronal intranuclear inclusion disease: A very rare syndrome characterized mainly by muscle and nerve degeneration.
  • Oligohydramnios: An abnormally small amount of amniotic fluid surrounding the fetus during pregnancy.
  • Osteoarthritis: A form of degenerative arthritis due to chronic degeneration
  • Perphenazine -- Teratogenic Agent: There is evidence to indicate that exposure to Pentazocine during pregnancy may have a teratogenic effect on the fetus. A teratogen is a substance that can cause birth defects. The likelihood and severity of defects may be affected by the level of exposure and the stage of pregnancy that the exposure occurred at.
  • Pes planus: A collapse of the arch of the foot, leading to a flattening of the feet.
  • Renal agenesis, bilateral: A rare congenital malformation where the kidneys don't develop during the fetal stage resulting in insufficient amniotic fluid.
  • Rheumatoid arthritis: An autoimmune inflammatory condition which primarily affects the joints
  • Skeletal symptoms: Symptoms affecting the skeletal system such as the bones.
  • Spastic disorders: Brain disorders leading to sustained spasms, stiffness and rigidity
  • Spinal muscular atrophy, Ryukyuan type: A recessively inherited disorder occurring in males from a Japanese inhabitants of Ryukyu Islands. The disorder is characterized by muscle wasting and weakness that affects the lower legs more than the arms.
  • Spinocerebellar ataxia -- dysmorphism: A rare inherited syndrome characterized by ataxia and unusual facial appearance.
  • Talipes equinovarus: A congenital foot deformity where the end of the foot is abnormally angled, usually inwards and downwards. It often occurs due to crowding in the womb. The foot is unable to be placed flatly on the ground.
  • Tethered Spinal Cord Syndrome: Spinal cord condition from abnormally stretched spinal cord.
  • Townes-Brocks Syndrome: A rare condition characterized by anal, hand, foot and ear abnormalities.
  • Trisomy 18 Syndrome: A rare genetic chromosomal syndrome where the child has an extra third copy of chromosome 18. Most fetuses are aborted before term, but a live birth with this condition occurs with a frequency around 1-in-3000. Edwards syndrome is more severe than the more common Down syndrome. Edwards syndrome causes mental retardation and numerous physical defects that often cause an early infant death. The condition has variable severity depending on how many of the body's cells have the extra chromosome and how much of the extra chromosome is duplicated. In severe forms all cells have an extra copy of the complete chromosome 18 whereas milder forms may have only some cells having the extra chromosome. Other mild forms may have an extra copy of only part of chromosome 18 in some or all of the body cells.
  • Weaver Syndrome: A syndrome that is considered a variant of the Marshall-Smith syndrome
  • Ziehen-Oppenheim syndrome: A very rare genetic condition involving progressive spasming of the muscles causing the body to twist and turn.

Conditions listing medical symptoms: Foot deformities:

The following list of conditions have 'Foot deformities' 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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Conditions listing medical complications: Foot deformities:

The following list of medical conditions have 'Foot deformities' or similar listed as a medical complication in our database.

 

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