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Sorghum-associated arthrogryposis and axonopathy is a rare congenital condition reported in ruminants and horses. Here, we describe the epidemiologic, clinical, and pathologic aspects of nine outbreaks of this condition in beef cattle in midwestern and southeastern Brazil (2014-2023). These regions are the most productive grain sorghum areas, where livestock producers use the straw extensively, producing a high regrowth during drought periods. All the affected pregnant cows had grazed sorghum stover for periods ranging from 25 days to 4 months. They showed abortion in the final and middle third of gestation or gave birth to calves with arthrogryposis, with overflexion or overextension of the limbs. No other gross lesions were observed. Typical neurohistologic lesions in four autopsied calves from different outbreaks included scarce to numerous axonal spheroids in the gray matter of the dorsal and ventral horns in the cervical spinal cord. Ultrastructurally, degenerated axons exhibited a segmental accumulation of residual bodies and degenerate organelles. The combination of sorghum stover consumption by the dams and characteristic spinal cord lesions in affected calves is distinctive and confirms the diagnosis. Sorghum consumption in the region was also associated with acute poisoning and cystitis-ataxia syndrome. For the first time in the Americas, we report a sorghum-associated congenital syndrome characterized by arthrogryposis and axonopathy in beef cattle.
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http://dx.doi.org/10.1016/j.toxicon.2025.108439 | DOI Listing |
Toxicon
September 2025
Programa de Pós-graduação em Ciências Animais, Universidade de Brasília (UnB), Distrito Federal, Brazil; Plataforma de Investigación en Salud Animal (PSA), Instituto Nacional de Investigación Agropecuaria (INIA), Tacuarembó, Uruguay. Electronic address:
Sorghum-associated arthrogryposis and axonopathy is a rare congenital condition reported in ruminants and horses. Here, we describe the epidemiologic, clinical, and pathologic aspects of nine outbreaks of this condition in beef cattle in midwestern and southeastern Brazil (2014-2023). These regions are the most productive grain sorghum areas, where livestock producers use the straw extensively, producing a high regrowth during drought periods.
View Article and Find Full Text PDFToxicon
July 2025
Programa de Pós-graduação em Ciências Animais, Universidade de Brasília (UnB), Distrito Federal, Brazil; Plataforma de Investigación en Salud Animal (PSA), Instituto Nacional de Investigación Agropecuaria (INIA), Tacuarembó, Uruguay. Electronic address:
We reviewed the history, epidemiology, clinical signs, pathology, pathogenesis, treatment, control, and prophylaxis of Sorghum poisoning in livestock. Economic losses in the livestock industry associated with sorghum have been reported since the 19th century. Hyperacute/acute poisoning associated with cyanide (HCN) or nitrate/nitrite frequently occurs in ruminants that consume high quantities of growth and regrowth sorghum after drought, followed by rainfall, respectively.
View Article and Find Full Text PDFChildren (Basel)
May 2022
Department of Pediatrics, University of Lübeck, Ratzeburger Allee 160, 23538 Lübeck, Germany.
Lethal congenital contracture syndrome 11 (LCCS11) is a form of arthrogryposis multiplex congenita (AMC) which is associated with mutations in the gliomedin gene (GLDN) and has been known to be severely life-shortening, mainly due to respiratory insufficiency. Patients with this condition have been predominantly treated by pediatricians as they usually do not survive beyond childhood. In this case report, we present a young adult who developed severe progressive respiratory insufficiency as a teenager due to diaphragmatic hypomotility and was diagnosed with LCCS11 following the discovery of compound heterozygous pathogenic variants in GLDN.
View Article and Find Full Text PDFChildren (Basel)
October 2021
Department of Neurology, National Institute of Mental Health and Neuro-Sciences, Bengaluru 560029, India.
Distal arthrogryposis type 5D (DA5D), a rare autosomal recessive disorder, is caused by mutations in We describe two consanguineous families (three patients) with novel gene mutations detected by next-generation sequencing (NGS). A 12-year-old boy (patient 1) presented with birth asphyxia, motor developmental delay, multiple joint contractures, pes planus, kyphoscoliosis, undescended testis, hypophonic speech with a nasal twang, asymmetric ptosis, facial weakness, absent abductor pollicis brevis, bifacial, and distal lower limb weakness. Muscle MRI revealed asymmetric fatty infiltration of tensor fascia lata, hamstring, lateral compartment of the leg, and gastrocnemius.
View Article and Find Full Text PDFNeuromuscul Disord
January 2019
Centre de Référence de Pathologie Neuromusculaire Nord/Est/Ile de France, Institut de Myologie, CHU La Pitié-Salpêtrière, APHP, Paris, France.
PIEZO2 mutations have been described in dominant arthrogryposis, but homozygous mutations of PIEZO2 may also be responsible for more complex clinical patterns, associating distal arthrogryposis, neonatal respiratory insufficiency, scoliosis and proprioceptive impairment. We report here two sisters presenting with these clinical and genetic features. They had a similar phenotype, with severe hypotonia and respiratory distress at birth, delayed acquisition of motor milestones and need of scoliosis surgery.
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