Background. Arthrogryposis is a heterogeneous group of problems of the musculoskeletal system, clinically characterized by multiple contractures of the joints of at least two anatomical regions, presenting at birth. The aim of our study was to evaluate the results of a therapeutic approach to patients at the University Pediatric Orthopedic Clinic in Bratislava. Material and methods. Nineteen patients (13 girls, 6 boys) were treated and followed up between 1993 and 2004. Results. Six patients had a clear clinical appearance of classical arthrogryposis multiplex congenita, six had distal arthrogryposis, two girls had Larsen's syndrome, and three had other forms of joint involvement. At a mean age of 18.4 months (range, 9-52 months), 77 surgeries had been performed. Most of the surgical procedures were for clubfoot-like deformities and vertical talus (45 operations) and for hip dislocations (20 operations). All patients who underwent surgery for hip dislocations achieved a full range of hip movement after subsequent physiotherapy. Surgery on the other hip also had good functional outcome. At the last examination, all patients were independently ambulatory, but some (mainly the younger ones) needed help in feeding, hygiene or dressing. Conclusions. In our experience with this group of patients, physiotherapy and occupational therapy supported by orthotic equipment is an inseparable part of their lives. Complementary surgery gives an opportunity to improve the correction of deformities in cases where conservative treatment does not meet the needs of the patient, because their normal intellect gives them the potential for an almost normal adult life.
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Clin Genet
January 2025
Division of Genetics, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Arthrogryposis multiplex congenita (AMC) is a heterogeneous disorder associated with 1/3000 to 1/5000 live births. We report a consanguineous family with multiple affected members with AMC and identified a recessive mutation in the highly conserved splice donor site, resulting in the mis-splicing of the affected exons. SENP7 is a deSUMOylase that is critical for sarcomere assembly and skeletal muscle contraction by regulating the transcriptional program in the skeletal muscle.
View Article and Find Full Text PDFOrphanet J Rare Dis
December 2024
Faculty of Medicine, University of Ljubljana, Ljubljana, Slovenia.
Background: Arthrogryposis-renal dysfunction-cholestasis (ARC) syndrome, a rare autosomal recessive disorder, exhibits genetic heterogeneity with the VIPAS39 gene pathological variants being a distinct contributor.
Results: We present two related patients from Kosovo, describing the clinical, genetic, and therapeutic aspects of the syndrome. The identified novel VIPAS39 pathological variants (c.
Am J Med Genet A
December 2024
Division of Medical Genetics, Department of Specialized Medicine, McGill University Health Centre, Montreal, Quebec, Canada.
Biallelic variants in GLDN have recently been associated with lethal congenital contracture syndrome 11 (LCCS11), a form of fetal akinesia deformation sequence (FADS) with high neonatal mortality. In this report, we describe five individuals from two Canadian Inuit families originating from different communities in Nunavik all affected with FADS and harboring a rare homozygous missense variant, [NM_181789.4:c.
View Article and Find Full Text PDFInt J Mol Sci
December 2024
Laboratoire de Génétique Moléculaire, Centre Hospitalier Universitaire de Montpellier, 34093 Montpellier, France.
Congenital titinopathies reported to date show autosomal recessive inheritance and are caused by a variety of genomic variants, most of them located in metatranscript (MTT)-only exons. The aim of this study was to describe additional patients and establish robust genotype-phenotype associations in titinopathies. This study involved analyzing molecular, clinical, pathological, and muscle imaging features in 20 patients who had at least one pathogenic or likely pathogenic variant in MTT-only exons, with onset occurring antenatally or in the early postnatal stages.
View Article and Find Full Text PDFEur J Obstet Gynecol Reprod Biol
December 2024
Department of Neonatology, All India Institute of Medical Sciences, Bhubaneswar, Odisha 751019, India. Electronic address:
Background: Arthrogryposis multiplex congenita involves joint contractures across various body parts. Distal arthrogryposis type 5D (DA5D) is a rare, autosomal recessive subtype affecting distal extremities, with symptoms like knee extension contractures, camptodactyly, overriding fingers, ulnar wrist deviation, and scoliosis.
Case: A 24-year-old pregnant woman with a second-degree relative partner had a fetus showing increased nuchal translucency (3.
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