Search engine for discovering works of Art, research articles, and books related to Art and Culture
ShareThis
Javascript must be enabled to continue!

Clinical perspectives on myopathic complications in nephropathic cystinosis

View through CrossRef
Abstract Patients with nephropathic cystinosis are now living into their 50s and beyond thanks to advances in medical management. Due to this shift in the natural history of the disease, monitoring for and addressing extrarenal manifestations, including myopathy, has emerged as an area of increasing importance. Muscle involvement typically begins before the onset of noticeable symptoms, and evidence suggests that subtle signs may even emerge in childhood. The origin of muscle involvement in cystinosis has not fully been elucidated and is likely multifactorial. Nonetheless, cellular toxicity due to intralysosomal cystine accumulation appears to be a key catalyst. Myopathy in cystinosis, which can lead to muscle weakness, dysphagia, and pulmonary dysfunction, contributes to significant morbidity and mortality, including impaired quality of life, reduced ability to independently perform activities of daily living, feeding difficulties and malnutrition, choking, and aspiration. Nephrologists typically act as the de facto primary cystinosis providers and are tasked with screening for muscle involvement and coordinating multispecialty referrals to neurology, pulmonology, gastroenterology, and physical, occupational, and speech therapy. In this review, we aim to summarize the current understanding of myopathy in nephropathic cystinosis and discuss strategies to support monitoring, assessment, management, and mitigation of this complication, as well as specialist referral and coordination.
Title: Clinical perspectives on myopathic complications in nephropathic cystinosis
Description:
Abstract Patients with nephropathic cystinosis are now living into their 50s and beyond thanks to advances in medical management.
Due to this shift in the natural history of the disease, monitoring for and addressing extrarenal manifestations, including myopathy, has emerged as an area of increasing importance.
Muscle involvement typically begins before the onset of noticeable symptoms, and evidence suggests that subtle signs may even emerge in childhood.
The origin of muscle involvement in cystinosis has not fully been elucidated and is likely multifactorial.
Nonetheless, cellular toxicity due to intralysosomal cystine accumulation appears to be a key catalyst.
Myopathy in cystinosis, which can lead to muscle weakness, dysphagia, and pulmonary dysfunction, contributes to significant morbidity and mortality, including impaired quality of life, reduced ability to independently perform activities of daily living, feeding difficulties and malnutrition, choking, and aspiration.
Nephrologists typically act as the de facto primary cystinosis providers and are tasked with screening for muscle involvement and coordinating multispecialty referrals to neurology, pulmonology, gastroenterology, and physical, occupational, and speech therapy.
In this review, we aim to summarize the current understanding of myopathy in nephropathic cystinosis and discuss strategies to support monitoring, assessment, management, and mitigation of this complication, as well as specialist referral and coordination.

Related Results

“A Review Article On: Cystinosis”
“A Review Article On: Cystinosis”
A rare autosomal recessive condition called cystinosis is characterized by a buildup of cystine in the lysosomes. The transfer of cystine from the lysosomes into the cytosol is dis...
Neuroretinal structure changes in infantile nephropathic cystinosis
Neuroretinal structure changes in infantile nephropathic cystinosis
Abstract Background The aim of this study was to investigate the neuroretinal structure of patients with the lysosomal storage disease cystinosis...
A Personal History of Cystinosis by Dr. Jerry Schneider
A Personal History of Cystinosis by Dr. Jerry Schneider
Cystinosis is a rare lysosomal storage disease that is tightly linked with the name of the American physician and scientist Dr. Jerry Schneider. Dr. Schneider (1937–2021) received ...
Infantile Nephropathic Cystinosis in Sulaimani Pediatric Teaching Hospital: A Retrospective Cohort Study
Infantile Nephropathic Cystinosis in Sulaimani Pediatric Teaching Hospital: A Retrospective Cohort Study
Cystinosis is a rare metabolic autosomal recessive disorder which characterized by intralysosomal accumulation of cystine. There are three forms; infantile nephropathic is the comm...
Uncovering the Prevalence of Cystinosis through Genetic Analysis
Uncovering the Prevalence of Cystinosis through Genetic Analysis
Abstract Background Cystinosis is a metabolic disease characterized by the accumulation of cystine most of...
Hematopoietic Stem Cell Gene Therapy for Cystinosis: From Bench-to-Bedside
Hematopoietic Stem Cell Gene Therapy for Cystinosis: From Bench-to-Bedside
Cystinosis is an autosomal recessive metabolic disease that belongs to the family of lysosomal storage disorders. The gene involved is the CTNS gene that encodes cystinosin, a seve...
Newborn Screening: Review of its Impact for Cystinosis
Newborn Screening: Review of its Impact for Cystinosis
Newborn screening (NBS) programmes are considered to be one of the most successful secondary prevention measures in childhood to prevent or reduce morbidity and/or mortality via ea...
Neuropathic Cystinosis: A Rare Case Report
Neuropathic Cystinosis: A Rare Case Report
Cystinosis is a lysosomal storage disease characterized by an intracellular accumulation of cystine in different organs and tissues, leading to potentially severe organ dysfunction...

Back to Top