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Spondylocostal dysostosis (SCDO) is a rare condition characterized by short-trunk dwarfism secondary to developmental anomalies of the vertebrae and ribs. Previously the condition Jarcho-Levin syndrome (also known as spondylothoracic dysostosis) was grouped together with spondylocostal dysostosis, but the two diseases are now considered to be distinct entities.
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A rare condition, almost 400 cases of spondylocostal dysostosis have been described in the literature 1.
Spondylocostal dysostosis is characterized by a short-trunk dwarfism phenotype (normal length upper and lower limbs with a disproportionately-reduced size central body and short neck) due to maldevelopment of the vertebrae and ribs. A mild kyphoscoliosis is often present.
The abnormal development of the ribs including absent (rarely increased number), malalignment and/or fused ribs, such that overall there is a constricted thorax (narrow fetal thorax) leading to breathing difficulties, which can be life-threatening. Due to a lack of room in which to inflate, the lungs expand inferiorly, pushing down on the abdominal viscera resulting in secondary herniation, including umbilical, diaphragmatic, and inguinal hernias.
Vertebral anomalies occur at all levels of the spine, including:
Associated abnormalities include cardiac and genitourinary anomalies, and occasionally neural tube defects (including spinal dysraphism and Chiari malformation).
Primarily the disease is autosomal recessive, although rarer autosomal dominant forms have been described. Mutations have been found in genes coding for proteins from the Notch signaling pathway. This pathway is important in the process of somite segmentation, central to the development of the vertebrae and ribs. Mutations in the genes DLL3, MESP2, LFNG, and HES7, account for the respective clinicoradiological types 1-4 i.e. SCDO1 to SCDO4.
Treatment and prognosis
The small size of the thorax in newborns frequently leads to respiratory compromise and death in infancy. Some rare variants with survival into adulthood have also been described.
History and Etymology
Saul Jarcho and Paul Levin first described the condition at Johns Hopkins in 1938 4. The condition that they described most closely resembles SCDO2 although Jarcho-Levin syndrome is now usually reserved for cases of spondylothoracic dysotosis 5.
- 1. Valeur, N., Iyer, R. and Ishak, G. (2016). Mind the gap: an unusual case of a cervical lipomyelocele. Radiology Case Reports, 11(3), pp.266-270. doi: 10.1016/j.radcr.2016.04.008.
- 2. Çetinkaya, M., Özkan, H., Köksal, N., Yazc, Z. and Yalçnkaya, U. (2008). Spondylocostal dysostosis associated with diaphragmatic hernia and neural tube defects. Clinical Dysmorphology, 17(2), pp.151-154. PMID: 18388793 DOI: 10.1097/MCD.0b013e3282f2699c
- 3. Anjankar, S. and Subodh, R. (2014). Spondylocostal dysostosis with lipomyelomeningocele: Case report and review of the literature. Journal of Pediatric Neurosciences, 9(3), p.249. doi: 10.4103/1817-1745.147580
- 4. Jarcho S, Levin P. (1938). Hereditary malformation of the vertebral bodies. Bull Johns Hopkins Hosp. 62, pp 216–26.
- 5. Turnpenny PD, Young E; ICVS (International Consortium for Vertebral Anomalies and Scoliosis). In: Pagon RA, Adam MP, Ardinger HH, Wallace SE, Amemiya A, Bean LJH, Bird TD, Ledbetter N, Mefford HC, Smith RJH, Stephens K, editors. SourceGeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2017. 2009 Aug 25 [updated 2013 Jan 17].