AI Article Synopsis

  • Jarcho-Levin syndrome is a rare genetic disorder marked by irregularities in vertebrae and rib structures, presenting symptoms like short neck, short trunk, and specific skeletal anomalies.
  • A case report details a one-day-old baby girl exhibiting these characteristics along with splenic herniation, highlighting a unique instance not previously documented in literature.
  • Early diagnosis through clinical and radiological assessment is crucial, with prenatal ultrasounds recommended for effective management, which includes neonatal care and potential spinal surgery to address breathing difficulties.

Article Abstract

BACKGROUND Jarcho-Levin syndrome, also known as spondylothoracic dysplasia and spondylocostal dysplasia, is characterized by varieties of vertebrae and rib anomalies. Jarcho-Levin syndrome is a clinical-radiological diagnosis with clinical evidence of short neck, short trunk, normal-sized limbs, or increased arm span, and vertebral and rib defects on the skeletal survey. CASE REPORT About 400 cases have been reported in world literature and 18 in our Indian literature. We report the case of a one-day-old female baby with a short trunk, short neck, low hairline, apparently long limbs, protuberant abdomen, mild midfacial dysmorphism, low-set ears, and a high-arched palate. There was one cystic swelling over the lateral side of the left hypochondrium sized about 3×3 centimeters, nonpusatile; the skin over the swelling was normal color and free. Radiological findings showed crowding of ribs with pebble-like appearance of the vertebrae and diastematomyelia of the spinal cord (type 2). We report here the first case of Jarcho-Levin syndrome with splenic herniation. To the best of our knowledge there have been no case reports of Jarcho-Levin syndrome with splenic herniation in the literature. CONCLUSIONS Jarcho-Levin syndrome can be easily diagnosed by clinical-radiological findings in newborns, with short trunk having a high index of suspicion. Prenatal diagnosis using level 2 ultrasonography can make it easier to manage the baby after delivery. Management should be from the basic neonatal care to prevention and immediate treatment of recurrent respiratory infections. Spinal surgical intervention to improve the thoracic volume and hence decrease the pulmonary restriction has been tried.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5067110PMC
http://dx.doi.org/10.12659/ajcr.898165DOI Listing

Publication Analysis

Top Keywords

jarcho-levin syndrome
24
syndrome splenic
12
splenic herniation
12
short trunk
12
short neck
8
report case
8
jarcho-levin
6
syndrome
5
short
5
herniation rare
4

Similar Publications

Article Synopsis
  • Spondylocostal dysostosis (SCD) is a genetic disorder leading to vertebrae and rib abnormalities, resulting in complications like kyphoscoliosis and lung issues.* -
  • A case study discusses a pregnant woman with severe kyphoscoliosis and lung problems who safely underwent cesarean delivery using modified anesthesia techniques.* -
  • The report highlights the importance of tailored anesthetic strategies for patients with SCD to ensure safety during surgical procedures.*
View Article and Find Full Text PDF

Case: We describe treatment of severe multilevel congenital thoracic fusion in a 3-year-old girl with Apert Syndrome by posterior element excision, posterior column osteotomies, and gradual distraction with magnetically controlled growing rods (MCGR) with 3-year follow-up. We also describe short-term follow-up with similar management in an 8-year-old patient with a congenitally fused thoracic spine from Jarcho-Levin syndrome.

Conclusion: Posterior element resection and targeted posterior column osteotomies combined with gradual distraction with MCGR offers a promising treatment course for children with severe thoracic insufficiency syndrome derived from congenital fusions.

View Article and Find Full Text PDF
Article Synopsis
  • Spondylocostal dysostosis (Jarcho Levin syndrome) is a rare condition affecting the spine and ribs, causing breathing difficulties from birth.
  • The report discusses an infant diagnosed with both spondylocostal dysostosis and type II split cord malformation, utilizing CT and MRI for detection.
  • It also includes a summary of other documented cases of patients with these two combined conditions from previous research.
View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!