Juvenile multiple sclerosis: addressing epidemiology, diagnosis, therapeutic, and prognostic updates along with cognitive dysfunction and quality of life
Juvenile multiple sclerosis (JMS) is a rare but significant subtype of multiple sclerosis (MS) that affects a small percentage of patients under the age of 10 and 3–5% of all MS patients. Despite its rarity, JMS poses unique challenges in terms of diagnosis, treatment, and management, as it can sign...
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| Veröffentlicht in: | Annals of medicine and surgery Jg. 85; H. 9; S. 4433 - 4441 |
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| Format: | Journal Article |
| Sprache: | Englisch |
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Hagerstown, MD
Lippincott Williams & Wilkins
01.09.2023
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| ISSN: | 2049-0801, 2049-0801 |
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| Abstract | Juvenile multiple sclerosis (JMS) is a rare but significant subtype of multiple sclerosis (MS) that affects a small percentage of patients under the age of 10 and 3–5% of all MS patients. Despite its rarity, JMS poses unique challenges in terms of diagnosis, treatment, and management, as it can significantly impact a child or adolescent’s physical, cognitive, and emotional development. JMS presents with a varying spectrum of signs and symptoms such as coordination difficulties and permanent cognitive dysfunctions and may include atypical clinical features such as seizures, acute disseminated encephalomyelitis, and optic neuritis, making diagnostic evaluations challenging. Whilst the biology of JMS shares similarities with adult-onset MS, there exist notable distinctions in disease progression, clinical manifestations, and ultimate prognoses. The International Pediatric MS Study Group (IPMSSG) was founded in 2005 to improve understanding of JMS, but there remains a lack of knowledge and guidelines on the management of this condition. This review summarizes the current knowledge on JMS, including its epidemiology, clinical presentations, diagnostic challenges, current treatment options, and outcomes. Current treatment options for JMS include disease-modifying therapies, but JMS can also result in impaired quality of life and psychiatric comorbidity, highlighting the need for comprehensive care for affected children. Through gathering and analyzing scattered studies and recent updates on JMS, the authors aim to address the gaps in current knowledge on JMS and provide an improved understanding of appropriate care for affected children. By doing so, this review hopes to contribute to improving the quality of life and outcomes for JMS patients. |
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| AbstractList | Juvenile multiple sclerosis (JMS) is a rare but significant subtype of multiple sclerosis (MS) that affects a small percentage of patients under the age of 10 and 3–5% of all MS patients. Despite its rarity, JMS poses unique challenges in terms of diagnosis, treatment, and management, as it can significantly impact a child or adolescent’s physical, cognitive, and emotional development. JMS presents with a varying spectrum of signs and symptoms such as coordination difficulties and permanent cognitive dysfunctions and may include atypical clinical features such as seizures, acute disseminated encephalomyelitis, and optic neuritis, making diagnostic evaluations challenging. Whilst the biology of JMS shares similarities with adult-onset MS, there exist notable distinctions in disease progression, clinical manifestations, and ultimate prognoses. The International Pediatric MS Study Group (IPMSSG) was founded in 2005 to improve understanding of JMS, but there remains a lack of knowledge and guidelines on the management of this condition. This review summarizes the current knowledge on JMS, including its epidemiology, clinical presentations, diagnostic challenges, current treatment options, and outcomes. Current treatment options for JMS include disease-modifying therapies, but JMS can also result in impaired quality of life and psychiatric comorbidity, highlighting the need for comprehensive care for affected children. Through gathering and analyzing scattered studies and recent updates on JMS, the authors aim to address the gaps in current knowledge on JMS and provide an improved understanding of appropriate care for affected children. By doing so, this review hopes to contribute to improving the quality of life and outcomes for JMS patients. Juvenile multiple sclerosis (JMS) is a rare but significant subtype of multiple sclerosis (MS) that affects a small percentage of patients under the age of 10 and 3-5% of all MS patients. Despite its rarity, JMS poses unique challenges in terms of diagnosis, treatment, and management, as it can significantly impact a child or adolescent's physical, cognitive, and emotional development. JMS presents with a varying spectrum of signs and symptoms such as coordination difficulties and permanent cognitive dysfunctions and may include atypical clinical features such as seizures, acute disseminated encephalomyelitis, and optic neuritis, making diagnostic evaluations challenging. Whilst the biology of JMS shares similarities with adult-onset MS, there exist notable distinctions in disease progression, clinical manifestations, and ultimate prognoses. The International Pediatric MS Study Group (IPMSSG) was founded in 2005 to improve understanding of JMS, but there remains a lack of knowledge and guidelines on the management of this condition. This review summarizes the current knowledge on JMS, including its epidemiology, clinical presentations, diagnostic challenges, current treatment options, and outcomes. Current treatment options for JMS include disease-modifying therapies, but JMS can also result in impaired quality of life and psychiatric comorbidity, highlighting the need for comprehensive care for affected children. Through gathering and analyzing scattered studies and recent updates on JMS, the authors aim to address the gaps in current knowledge on JMS and provide an improved understanding of appropriate care for affected children. By doing so, this review hopes to contribute to improving the quality of life and outcomes for JMS patients.Juvenile multiple sclerosis (JMS) is a rare but significant subtype of multiple sclerosis (MS) that affects a small percentage of patients under the age of 10 and 3-5% of all MS patients. Despite its rarity, JMS poses unique challenges in terms of diagnosis, treatment, and management, as it can significantly impact a child or adolescent's physical, cognitive, and emotional development. JMS presents with a varying spectrum of signs and symptoms such as coordination difficulties and permanent cognitive dysfunctions and may include atypical clinical features such as seizures, acute disseminated encephalomyelitis, and optic neuritis, making diagnostic evaluations challenging. Whilst the biology of JMS shares similarities with adult-onset MS, there exist notable distinctions in disease progression, clinical manifestations, and ultimate prognoses. The International Pediatric MS Study Group (IPMSSG) was founded in 2005 to improve understanding of JMS, but there remains a lack of knowledge and guidelines on the management of this condition. This review summarizes the current knowledge on JMS, including its epidemiology, clinical presentations, diagnostic challenges, current treatment options, and outcomes. Current treatment options for JMS include disease-modifying therapies, but JMS can also result in impaired quality of life and psychiatric comorbidity, highlighting the need for comprehensive care for affected children. Through gathering and analyzing scattered studies and recent updates on JMS, the authors aim to address the gaps in current knowledge on JMS and provide an improved understanding of appropriate care for affected children. By doing so, this review hopes to contribute to improving the quality of life and outcomes for JMS patients. |
| Author | Inban, Pugazhendi Natarajan, Balaganesh Amir Hussin, Omniat John, Jobby Sowndarya, Dommaraju Vaja, HariOm Prajjwal, Priyadarshi Gadam, Srikanth A.D.M., Marsool M.D.M., Marsool Abbas, Rahim |
| AuthorAffiliation | c Somervell Memorial CSI Medical College and Hospital, Karakonam, Trivandrum b Internal Medicine, Government Medical College, Omandurar, Chennai a Neurology, Bharati Vidyapeeth University Medical College Pune e Odessa National Medical University, Odessa, Ukraine h St. George’s University School of Medicine, University Centre Grenada, West Indies g Asfendiyarov Kazakh National Medical University, Almaty, Kazakhstan i Internal Medicine, Postdoctoral Research Fellow, Mayo Clinic, USA d Internal Medicine, BJ Medical College, Ahmedabad, India f University of Baghdad, Al-Kindy College of Medicine, Baghdad, Iraq j Internal Medicine, Al-Manhal Academy, Khartoum, Sudan |
| AuthorAffiliation_xml | – name: h St. George’s University School of Medicine, University Centre Grenada, West Indies – name: f University of Baghdad, Al-Kindy College of Medicine, Baghdad, Iraq – name: j Internal Medicine, Al-Manhal Academy, Khartoum, Sudan – name: d Internal Medicine, BJ Medical College, Ahmedabad, India – name: a Neurology, Bharati Vidyapeeth University Medical College Pune – name: c Somervell Memorial CSI Medical College and Hospital, Karakonam, Trivandrum – name: b Internal Medicine, Government Medical College, Omandurar, Chennai – name: i Internal Medicine, Postdoctoral Research Fellow, Mayo Clinic, USA – name: g Asfendiyarov Kazakh National Medical University, Almaty, Kazakhstan – name: e Odessa National Medical University, Odessa, Ukraine |
| Author_xml | – sequence: 1 givenname: Priyadarshi surname: Prajjwal fullname: Prajjwal, Priyadarshi organization: Neurology, Bharati Vidyapeeth University Medical College Pune – sequence: 2 givenname: Marsool surname: M.D.M. fullname: M.D.M., Marsool organization: University of Baghdad, Al-Kindy College of Medicine, Baghdad, Iraq – sequence: 3 givenname: Balaganesh surname: Natarajan fullname: Natarajan, Balaganesh organization: St. George’s University School of Medicine, University Centre Grenada, West Indies – sequence: 4 givenname: Pugazhendi surname: Inban fullname: Inban, Pugazhendi organization: Internal Medicine, Government Medical College, Omandurar, Chennai – sequence: 5 givenname: Srikanth surname: Gadam fullname: Gadam, Srikanth organization: Internal Medicine, Postdoctoral Research Fellow, Mayo Clinic, USA – sequence: 6 givenname: Dommaraju surname: Sowndarya fullname: Sowndarya, Dommaraju organization: Odessa National Medical University, Odessa, Ukraine – sequence: 7 givenname: Jobby surname: John fullname: John, Jobby organization: Somervell Memorial CSI Medical College and Hospital, Karakonam, Trivandrum – sequence: 8 givenname: Rahim surname: Abbas fullname: Abbas, Rahim organization: Asfendiyarov Kazakh National Medical University, Almaty, Kazakhstan – sequence: 9 givenname: HariOm surname: Vaja fullname: Vaja, HariOm organization: Internal Medicine, BJ Medical College, Ahmedabad, India – sequence: 10 givenname: Marsool surname: A.D.M. fullname: A.D.M., Marsool organization: University of Baghdad, Al-Kindy College of Medicine, Baghdad, Iraq – sequence: 11 givenname: Omniat orcidid: 0000-0002-5021-263X surname: Amir Hussin fullname: Amir Hussin, Omniat organization: Internal Medicine, Al-Manhal Academy, Khartoum, Sudan |
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| CitedBy_id | crossref_primary_10_1016_j_neuint_2023_105645 crossref_primary_10_1007_s00112_023_01890_9 crossref_primary_10_1016_j_msard_2024_106162 crossref_primary_10_1080_09273948_2024_2414917 |
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