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  2. Congenital vertebral anomaly - Wikipedia

    en.wikipedia.org/wiki/Congenital_vertebral_anomaly

    Lumbarization is an anomaly in the spine. It is defined by the nonfusion of the first and second segments of the sacrum. The lumbar spine subsequently appears to have six vertebrae or segments, not five. This sixth lumbar vertebra is known as a transitional vertebra. Conversely the sacrum appears to have only four segments instead of its ...

  3. Bertolotti's syndrome - Wikipedia

    en.wikipedia.org/wiki/Bertolotti's_syndrome

    Bertolotti's syndrome is a commonly missed cause of back pain which occurs due to lumbosacral transitional vertebrae (LSTV). It is a congenital condition but is not usually symptomatic until one's later twenties or early thirties. [1] However, there are a few cases of Bertolotti's that become symptomatic at a much earlier age.

  4. Klippel–Feil syndrome - Wikipedia

    en.wikipedia.org/wiki/Klippel–Feil_syndrome

    The three categories treated for types of spinal cord deficiencies are massive fusion of the cervical spine (Type I), the fusion of 1 or 2 vertebrae (Type II), and the presence of thoracic and lumbar spine anomalies in association with type I or type II Klippel–Feil syndrome (Type III). [citation needed]

  5. Spina bifida - Wikipedia

    en.wikipedia.org/wiki/Spina_bifida

    Spina bifida (SB; /ˌspaɪnə ˈbɪfɪdə/, [9] Latin for 'split spine') [10] is a birth defect in which there is incomplete closing of the spine and the membranes around the spinal cord during early development in pregnancy. [1] There are three main types: spina bifida occulta, meningocele and myelomeningocele. [1]

  6. Category : Congenital disorders of musculoskeletal system

    en.wikipedia.org/wiki/Category:Congenital...

    This category reflects the organization of International Statistical Classification of Diseases and Related Health Problems, 10th Revision. Generally, diseases outlined within the ICD-10 codes Q65-Q79 within Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities should be included in this category.

  7. VACTERL association - Wikipedia

    en.wikipedia.org/wiki/VACTERL_association

    Vertebral anomalies, or defects of the spinal column, usually consist of small (hypoplastic) vertebrae or hemivertebra where only one half of the bone is formed.About 80 percent of patients with VACTERL association will have vertebral anomalies. [6]

  8. Diastematomyelia - Wikipedia

    en.wikipedia.org/wiki/Diastematomyelia

    Diastematomyelia is a "dysraphic state" of unknown embryonic origin, but is probably initiated by an accessory neurenteric canal (an additional embryonic spinal canal.).) This condition may be an isolated phenomenon or may be associated with other segmental anomalies of the vertebral bodies such as spina bifida, kyphoscoliosis, butterfly vertebra, hemivertebra and block vertebrae which are ...

  9. Pascual-Castroviejo syndrome type 1 - Wikipedia

    en.wikipedia.org/wiki/Pascual-Castroviejo...

    Coffin syndrome patients have vertebral anomalies that contribute to kyphosis, but no rib deformities have been described, and facial dysmorphic traits are more evident. Similar dysmorphic traits have been described in Robinow syndrome, albeit many features, such as normal genitalia, mental impairment, and a lack of limb bone deformities, are ...