Background: Spinal Muscular Atrophy (SMA) is manifested by deformation of the chest wall, including a bell-shaped chest. We determined the ability of a novel non-ionizing, non-volitional method to measure and quantify bell-shaped chests in SMA.

Methods: A 3D depth camera and a chest x-ray (CXR) were used to capture chest images in 14 SMA patients and 28 controls. Both methods measure the distance between two points, but measurements performed by 3D analysis allow for the consideration of the curve of a surface (geodesic measurements), whereas the CXR allows solely for the determination of the shortest path between two points, with no regard for the surface (Euclidean measurements). The ratio of the upper to lower chest distances was quantified to distinguish chest shape in imaging by both the 3D depth camera and the CXR, and the ratios were compared between healthy and SMA patients.

Results: The mean 3D Euclidean ratio of distances measured by 3D imaging was 1.00 in the control group and 0.92 in the SMA group ( = 0.01), the latter indicative of a bell-shaped chest. This result repeated itself in the ratio of geodesic measurements (0.99 vs. 0.89, respectively,  = 0.03).

Conclusion: The herein-described novel, noninvasive 3D method for measuring the upper and lower chest distances was shown to distinguish the bell-shaped chest configuration in patients with SMA from the chests of controls. This method bears several advantages over CXR and may be readily applicable in clinical settings that manage children with SMA.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10876057PMC
http://dx.doi.org/10.3389/fped.2024.1256445DOI Listing

Publication Analysis

Top Keywords

bell-shaped chest
12
chest
9
bell-shaped chests
8
spinal muscular
8
muscular atrophy
8
depth camera
8
geodesic measurements
8
upper lower
8
lower chest
8
chest distances
8

Similar Publications

Article Synopsis
  • A female neonate born to consanguineous parents exhibited severe hyperparathyroidism (NSHPT) after a C-section, showing signs of respiratory distress and skeletal abnormalities following birth.
  • Diagnostic challenges included elevated calcium levels and a homozygous variant in the calcium-sensing receptor (CaSR) gene, leading to the establishment of NSHPT.
  • Management of NSHPT is critical due to its high mortality risk; treatment options typically involve addressing the high calcium levels and associated metabolic issues.
View Article and Find Full Text PDF

Shanidar 3 'rings the bell': Virtual ribcage reconstruction and its implications for understanding the Neanderthal bauplan.

J Hum Evol

December 2024

Paleoanthropology Group, Department of Paleobiology, Museo Nacional de Ciencias Naturales (MNCN-CSIC), Calle José Gutiérrez Abascal, 2, 28006, Madrid, Spain.

The study of the ribcage is fundamental to understanding hominin evolution. However, ribs and vertebrae are scarce in the fossil record. Although Neanderthals are one of the most represented and, therefore, one of the most studied fossil Homo species, it is controversial whether there is a standardized Neanderthal ribcage morphotype that could differ from modern humans.

View Article and Find Full Text PDF

Jeune syndrome, a rare autosomal recessive disorder, is characterized by skeletal abnormalities, particularly a narrow, bell-shaped chest, leading to severe respiratory distress in newborns. This case report details a full-term female neonate presenting with significant respiratory challenges, typical skeletal features, and early-onset renal dysfunction. Despite normal initial imaging, persistent renal abnormalities were observed, underscoring the need for early diagnosis, vigilant monitoring, and a multidisciplinary management approach to optimize outcomes for patients with Jeune syndrome.

View Article and Find Full Text PDF

Prenatal diagnosis of recurrent Kagami-Ogata syndrome inherited from a mother affected by Temple syndrome: a case report and literature review.

BMC Med Genomics

August 2024

Department of Obstetrics and Gynecology, National Clinical Research Center for Obstetric & Gynecologic Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Science & Peking Union Medical College, Beijing, China.

Article Synopsis
  • Kagami-Ogata syndrome (KOS) and Temple syndrome (TS) are rare genetic disorders linked to imprinted genes on chromosome 14q32, affecting maternal and paternal gene expression, respectively.
  • A unique case involved a mother with TS who had two pregnancies with KOS, showing symptoms like prenatal overgrowth and omphalocele, confirmed by genetic testing revealing a deletion in the imprinted region.
  • Proper prenatal diagnosis of KOS relies on better recognition of its symptoms by healthcare providers and the significance of studying imprinted gene regions in genetic lab tests.
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!