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Symptoms » Flattened vertebrae » Glossary
 

Glossary for Flattened vertebrae

Medical terms related to Flattened vertebrae or mentioned in this section include:

  • Akaba-Hayasaka syndrome: A very rare syndrome characterized mainly by a prominent forehead, cloudy corneas, low nasal bridge, underdeveloped chest and short limbs.
  • Anauxetic dysplasia: A rare disorder characterized by abnormal skeletal and spinal development.
  • Back symptoms: Symptoms affecting the back
  • Bone symptoms: Symptoms affecting the body's bones
  • Brachyolmia: A syndrome characterized mainly by short trunk dwarfism. There are several different subtypes, each with different additional features.
  • Campomelic dwarfism: A rare genetic disorder characterized by bowed tibia, underdeveloped shoulder blades and a flat face.
  • Cantu Sanchez-Corona Garcia-cruz syndrome: A rare syndrome characterized by mental retardation, short stature, large skull, heart anomaly and various other abnormalities.
  • Cardiomyopathy cataract hip spine disease: A rare genetic disorder characterized by heart muscle disease, cataracts and hip and spinal problems.
  • Dreyfus syndrome: A rare syndrome characterized by flattened vertebrae, kyphoscoliosis, spinal ankylosis, short neck, dwarfism and other abnormalities.
  • Dyggve-Melchior-Clausen Syndrome: A rare genetic bone growth disorder characterized by short stature and other skeletal deformities.
  • Facial dysmorphism -- intellectual deficit -- short stature -- hearing loss: A very rare inherited disorder characterized by retarded growth, mental retardation, bone abnormalities and distinctive facial features.
  • Fibrochondrogenesis: A rare genetic disorder characterized by short stature, abnormal bone formation and stillbirth or neonatal death.
  • Greenberg dysplasia: A very rare form of short-limbed dwarfism.
  • HEM dysplasia: A rare disorder characterized by hydrops, dwarfism and abnormal bone calcification. The condition generally results in fetal death.
  • Head symptoms: Symptoms affecting the head or brain
  • Hutterite cerebroosteonephrodysplasia syndrome: A very rare disorder characterized by short stature and a severe degenerative brain disorder.
  • Hypertrichotic osteochondrodysplasia: A rare syndrome characterized by mental retardation, short stature, large skull, heart anomaly and various other abnormalities.
  • Lumbar malsegmentation, short stature and facial anomalies: A rare syndrome characterized by vertebral abnormalities, short stature and facial anomalies.
  • MPS-IV (Morquio Disease): A condition which is characterized by biochemically distinct mucopolysaccharidosis
  • Metatrophic dysplasia: A very rare form of dwarfism involving short limbs and a long trunk. Less than 100 cases of the condition have been reported.
  • Microcephalic osteodysplastic primordial dwarfism types 1 and 3: Microcephalic osteodysplastic primordial dwarfism types 1 and 3 were originally regarded as separate conditions but it was recently concluded that they were different expressions of the same condition. The main differences between the two forms is a difference in the radiological bone anomalies. The condition is characterized mainly by bone abnormalities, short stature and a small head.
  • Musculoskeletal symptoms: Symptoms affecting muscles or bones of the skeleton.
  • Myhre Syndrome: A very rare inherited disorder characterized by retarded growth, mental retardation, bone abnormalities and distinctive facial features.
  • Myhre-Ruvalcaba-Graham syndrome: A rare disorder characterized by mental retardation, retarded growth before and after birth, early-onset deafness and facial anomalies as well as other problems.
  • 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.
  • Osteogenesis imperfecta type II: A rare lethal form of the genetic connective tissue disorder characterized by fragile bones, blue sclerae and facial and tooth abnormalities.
  • Osteogenesis imperfecta, type 2: A rare lethal form of the genetic connective tissue disorder characterized by fragile bones, blue sclerae and facial and tooth abnormalities.
  • Osteogenesis imperfecta, type 2A: A rare lethal form of a genetic connective tissue disorder characterized by fragile bones, blue sclerae and facial and tooth abnormalities. Type IIA has a different origin of the genetic mutation but the clinical features are similar. Type IIA involves a defect on the COL1A2 gene. The main difference is that type IIA tends to involve a large head and dark blue eyes.
  • Osteogenesis imperfecta, type IIB: A rare, recessively inherited, lethal form of a genetic connective tissue disorder characterized by fragile bones, blue sclerae and facial and tooth abnormalities. Type IIB has a different origin of the genetic mutation but the clinical features are similar. Type IIB involves a defect on the CRTAP gene on chromosome 3p22. The main difference is that type IIA tends to involve a small head and white or light blue eyes.
  • Otospondylomegaepiphyseal dysplasia: A rare genetic disorder where abnormal bone growth causes hearing loss, skeletal abnormalities and characteristic facial features.
  • Pseudoachondroplasia: A rare genetic disorder characterized by bone growth and development abnormalities.
  • Short limb dwarfism, Al Gazali type: A very rare lethal disorder involving severe limb shortening and other skeletal deformities.
  • Skeletal symptoms: Symptoms affecting the skeletal system such as the bones.
  • Spine symptoms: Symptoms affecting the spine
  • Spondylo-humero-femoral dysplasia: A rare genetic disorder characterized by bone formation abnormalities, short stature and early death.
  • Spondylo-ocular syndrome: A rare, recessively inherited syndrome characterized mainly by eye and spinal abnormalities.
  • Spondylodysplasia and Premature Pubarche: A very rare condition characterized by premature puberty and vertebral abnormalities.
  • Spondyloepimetaphyseal Dysplasia, Aggrecan Type: A very rare syndrome observed in 3 siblings and characterized primarily by various bone abnormalities.
  • Spondyloepimetaphyseal Dysplasia, Pakistani Type: A rare condition observed in a large family from Pakistani characterized by abnormal bone growth of a distinctive form.
  • Spondyloepimetaphyseal dysplasia congenita, Iraqi: A very rare syndrome characterized mainly by abnormal bone growth. Only a few cases have been reported.
  • Spondyloepimetaphyseal dysplasia with abnormal dentition: A rare skeletal disorder where the spine and long bones grow and develop abnormally. This particular type also involves tooth abnormalities.
  • Spondyloepimetaphyseal dysplasia, Irapa type: A rare skeletal disorder where the spine and long bones grow and develop abnormally resulting in a short spine, short hand and foot bones and flattened vertebrae.
  • Spondyloepimetaphyseal dysplasia, genevieve type: A recessively inherited disorder characterized mainly by abnormal bone development (epiphyses, metaphyses and vertebrae) as well as mental retardation. The abnormalities become progressively worse with age.
  • Spondyloepiphyseal dysplasia tarda: A rare genetic disorder characterized by short stature and skeletal abnormalities which are usually not apparent before 12 years.
  • Spondylometaphyseal dysplasia -- cone-rod dystrophy: A rare syndrome characterized by skeletal abnormalities (spine and metaphyses) and an eye disorder. Vision impairment starts early in life and tends to progress but often stabilizes during adolescence.
  • Spondylometaphyseal dysplasia, Sedaghatian type: A very rare syndrome characterized by abnormal bone development with short arms and flattened vertebrae. Death usually occurs within days of birth.
  • Spondylometaphyseal dysplasia, X-linked: A rare disorder characterized by spine and long bone abnormalities and facial anomalies. The disorder is inherited in a X-linked manner which means that males exhibit the full extent of the symptoms whereas female carriers often have only mild symptoms.
  • Spondylometaphyseal dysplasia, axial: A rare skeletal disorder involving abnormal bone development. The condition is characterized by flattened vertebrae, small rib cage, abnormal ribs and other bone abnormalities.
  • Swelling symptoms: Symptoms causing swelling or enlargement.
  • Thanatophoric dysplasia:
  • Thanatophoric dysplasia, type 1: A rare lethal genetic disorder characterized by severe skeletal abnormalities, flat vertebrae, large head and low nasal bridge.
  • Thanatophoric dysplasia, type 2: A rare lethal genetic disorder characterized by severe skeletal abnormalities, flat vertebrae, large head and low nasal bridge.
  • Vertebra symptoms: Symptoms affecting the vertebra or discs in the spine.

Conditions listing medical symptoms: Flattened vertebrae:

The following list of conditions have 'Flattened vertebrae' 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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