Juvenile Onset Causes & Reasons

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Juvenile Onset Symptom Checker: Possible causes include Limb-Girdle Muscular Dystrophy Type 1F. Check the full list of possible causes and conditions now! Talk to our Chatbot to narrow down your search.

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Possible Causes

Limb-Girdle Muscular Dystrophy Type 1F

Respiratory involvement was found in patients with juvenile-onset and severe phenotype. [link.springer.com]

The disease has generally a benign clinical course but some individuals with childhood or juvenile onset manifest severe widespread myopathy, leading to wheelchair dependency [uniprot.org]

Two forms were delineated based on age at onset: a juvenile form with onset before age 15 years (66 %) and an adult-onset form starting around the third or fourth decade [link.springer.com]

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Wolfram Syndrome

The authors report on one case of Wolfram syndrome, a rare condition, which is characterized by juvenile onset diabetes mellitus, diabetes insipidus, optic atrophy and sensorineural [ncbi.nlm.nih.gov]

Abstract Wolfram syndrome (WS), an infrequent cause of diabetes mellitus, derives its name from the physician who first reported the combination of juvenile-onset diabetes [ncbi.nlm.nih.gov]

Diagnostic methods The clinical criterion for WS diagnosis is juvenile-onset DM and OA, family history of WS or DM and D. [orpha.net]

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Juvenile Idiopathic Arthritis

Disease, Juvenile Onset, Still's Disease, Juvenile-Onset, Stills Disease, Juvenile-Onset, Juvenile-Onset Still Disease, STILL DISEASE JUVENILE ONSET, JUVENILE ONSET STILL [fpnotebook.com]

Abstract Systemic onset juvenile rheumatoid arthritis unresponsive to nonsteroidal anti-inflammatory drugs may be controlled with corticosteroids, but these drugs have significant [ncbi.nlm.nih.gov]

The aims of this study were to determine the expression of Fas antigen and Bcl-2 protein on peripheral blood T and B lymphocytes from patients with juvenile-onset systemic [ncbi.nlm.nih.gov]

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Juvenile Primary Lateral Sclerosis

[…] spastic paraplegia ; JALS juvenile-onset ALS ; JPLS juvenile-onset PLS ; NCS nerve conduction studies ; ND not done ; PLS primary lateral sclerosis ; SSEP somatosensory evoked [neurology.org]

A novel ALS2 splice-site mutation in a Cypriot juvenile-onset primary lateral sclerosis family. [ghr.nlm.nih.gov]

Juvenile-onset PLS (JPLS) is inherited in an autosomal recessive mode and is also found in sporadic cases. [neurology.org]

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Polyarticular Juvenile Idiopathic Arthritis

61 Spelling P...Pereira RM 18802807 2008 6 Mannose-binding lectin deficiency is associated with early onset of polyarticular juvenile rheumatoid arthritis: a cohort study. [malacards.org]

Childhood Arthritis and Rheumatology Research Alliance consensus treatment plans for new onset polyarticular juvenile idiopathic arthritis. [ncbi.nlm.nih.gov]

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Recurrent Respiratory Papillomatosis

Juvenile-onset recurrent respiratory papillomatosis is primarily a disease of children and adolescents. [ncbi.nlm.nih.gov]

Background Juvenile-onset recurrent respiratory papillomatosis (JORRP) is an infrequent but debilitating disease. [dx.doi.org]

Juvenile-onset recurrent respiratory papillomatosis (JORRP) is a rare disease associated with the human papilloma virus (HPV) in which papillomas form along the aerodigestive [ncbi.nlm.nih.gov]

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Infantile-Onset Ascending Hereditary Spastic Paralysis

Genotyping and linkage analyses demonstrated that this infantile-onset ascending hereditary spastic paralysis (IAHSP) is allelic to the condition previously reported as juvenile [ncbi.nlm.nih.gov]

We analyzed ALS2, recently found mutated in consanguineous Arabic families presenting either an ALS2 phenotype or juvenile-onset primary lateral sclerosis (JPLS), as a candidate [ncbi.nlm.nih.gov]

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Juvenile-Onset Still Disease

Juvenile onset Stills disease, also referred as systemic-onset juvenile idiopathic arthritis (SoJIA), occurs due to overstimulation of various proinflammatory cytokines, most [symptoma.com]

The topic Juvenile-Onset Still’s Disease you are seeking is a synonym, or alternative name, or is closely related to the medical condition Juvenile Rheumatoid Arthritis (JRA [dovemed.com]

Comparison of long term evolution of adult onset and juvenile onset Still's disease, both followed up for more than 10 years. [ard.bmj.com]

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Alexander Disease

We present here a 25-year-old woman with genetically confirmed (p.R276L mutation in the GFAP gene) juvenile-onset AxD. [ncbi.nlm.nih.gov]

Here we report on a single case of juvenile-onset Alexander disease associated with a novel frameshift mutation in the GFAP gene. [ncbi.nlm.nih.gov]

The nosology of putative juvenile-onset and adult-onset examples continues to be uncertain. [ncbi.nlm.nih.gov]

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Laryngeal Papilloma

All six adult onset cases carried HPV 6 sequences while the juvenile onset group comprised four HPV 6 and three HPV 11 cases. [ncbi.nlm.nih.gov]

[…] than juvenile-onset RRP. [journals.plos.org]

RRP may occur in adults (adult-onset RRP) as well as in infants and small children (juvenile-onset RRP) who may have contracted the virus during childbirth. [nidcd.nih.gov]

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Juvenile Huntington Disease

JUVENILE ONSET HUNTINGTON DISEASE ALTERNATE NAMES Juvenile Huntington Disease; Juvenile HD; JHD; Early-Onset HD DESCRIPTION Juvenile Onset Huntington Disease (JHD) is a form [secure.ssa.gov]

The mean age of onset for the siblings of juvenile onset cases is 26.8 years, which is significantly less than the mean age of onset (39.8) observed in siblings of non-juvenile [ncbi.nlm.nih.gov]

Furthermore, analysis of nuclear and extended families showed a familial predisposition to juvenile onset disease. [ncbi.nlm.nih.gov]

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Adult-Onset Still Disease

For the juvenile onset form see Systemic-onset juvenile idiopathic arthritis.Adult-onset Still's disease (AOSD) is a form of Still's disease, a rare systemic autoinflammatory [en.wikipedia.org]

ISSN 1546-0096 Abstract Background: Adult-onset Still’s disease (AOSD), a rare autoinflammatory disorder, resembles systemic juvenile idiopathic arthritis (SJIA). [ub.uni-heidelberg.de]

Comparison of long term evolution of adult onset and juvenile onset Still’s disease, both followed up for more than 10 years. Ann Rheum Dis. 1990;49:283–5. [doi.org]

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Neuronal Ceroid Lipofuscinosis

Infantile, juvenile, and adult-onset types with multiple genotype-phenotype associations have been described. [ncbi.nlm.nih.gov]

Abstract Three related patients from Colombia presented with a juvenile-onset neuronal ceroid lipofuscinosis. [n.neurology.org]

We describe a patient with juvenile-onset NCL phenotype with a new CLN1 mutation and deficient PPT activity. [ncbi.nlm.nih.gov]

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Juvenile Ankylosing Spondylitis

What is Juvenile-onset ankylosing spondylitis Statistics on Juvenile-onset ankylosing spondylitis Risk Factors for Juvenile-onset ankylosing spondylitis Progression of Juvenile-onset [myvmc.com]

Clinical, radiographic and functional differences between juvenile-onset and adult–onset ankylosing spondylitis: results from the PSOAS cohort L S Gensler 1, M M Ward 2, J [ard.bmj.com]

Prognosis of Juvenile-onset ankylosing spondylitis How is Juvenile-onset ankylosing spondylitis Treated? [myvmc.com]

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Juvenile Seronegative Polyarthritis

Other types of seronegative arthritis that are less commonly diagnosed include Dermatomyositis, enteropathic arthritis, juvenile onset or adult onset idiopathic arthritis, [rheumatoid-arthritis-decisions.com]

HLA and complement C4 antigens in polyarticular onset seronegative juvenile chronic arthritis: association of early onset with HLA-DRw8. J Rheumatol 1989;16:55–9. [link.springer.com]

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Metachromatic Leukodystrophy

We conclude that UCBT benefits children with pre-symptomatic early juvenile onset MLD by favourably altering the natural history of the disease. [ncbi.nlm.nih.gov]

In all, 7 patients, 4 with late infantile-onset and 3 with juvenile-onset disease, developed recurrent seizures. [ncbi.nlm.nih.gov]

Overall, children with juvenile onset had better outcomes than those with late-infantile onset. [ncbi.nlm.nih.gov]

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Cerulean Cataract

[…] extraction is generally necessary More General Terms autosomal dominant cataracts Internet Database OMIM: 610202 References OMIM [1] UniProt [2] congenital cerulean cataract 4 (juvenile-onset [anvita.info]

Lens opacities have a later, more juvenile onset and the lens opacities are located in a lamellar distribution in superficial cortical layers. [disorders.eyes.arizona.edu]

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Diabetes Mellitus Type 1

The aim of our study was to determine spontaneous apoptotic potential of the monocyte subsets in juvenile-onset complication-free diabetes mellitus type 1 and to compare them [ncbi.nlm.nih.gov]

Others considered a genetic explanation, whereby homozygous individuals with two copies of a hypothetical 'diabetes gene' developed juvenile onset diabetes, whereas those [diapedia.org]

What is Diabetes Mellitus Type 1 (insulin dependent, juvenile onset)? [healthengine.com.au]

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Neuronal Intranuclear Inclusion Disease

We present the clinicopathologic details of a patient with juvenile-onset NIID and discuss the pathogenesis. [ncbi.nlm.nih.gov]

Diagnostic considerations for juvenile onset Parkinsonism (onset at 21 years of age) include juvenile Huntington disease, Wilson disease, dentatorubral-pallidoluysian atrophy [ncbi.nlm.nih.gov]

CrossRef Google Scholar Access Volume 37, Issue 2 March 2010, pp. 213-218 Background: Diagnostic considerations for juvenile onset Parkinsonism (onset at Case Report: We present [cambridge.org]

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Pityriasis Rubra Pilaris

Classical juvenile -onset pityriasis rubra pilaris Circumscribed juvenile -onset pityriasis rubra pilaris How is pityriasis rubra pilaris diagnosed? [dermnetnz.org]

Classical juvenile-onset pityriasis rubra pilaris Circumscribed juvenile-onset pityriasis rubra pilaris How is pityriasis rubra pilaris diagnosed? [dermnetnz.org]

Adult pityriasis rubra pilaris Juvenile -onset PRP PRP in childhood can be classical ( generalised ) or circumscribed (limited in extent). [dermnetnz.org]

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Open-Angle Glaucoma

A genetic locus for juvenile onset primary open-angle glaucoma has been isolated to the long arm of chromosome 1. [ncbi.nlm.nih.gov]

We studied a consanguineous Pakistani family in which three affected individuals had a severe form of glaucoma with members in one generation diagnosed with juvenile-onset [ncbi.nlm.nih.gov]

To screen for mutations in the coding region of the myocilin (MYOC) gene in a large Malay family with juvenile-onset open angle glaucoma (JOAG). [ncbi.nlm.nih.gov]

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Best Disease

Abstract Recently, the VMD2 gene has been identified as the causative gene in juvenile-onset vitelliform macular dystrophy (Best disease), a central retinopathy primarily [ncbi.nlm.nih.gov]

Macular Dystrophy, Juvenile Onset [decs.bvs.br]

Adult-Onset Foveomacular Dystrophy, Adult-Onset, With Choroidal Neovascularization Juvenile-Onset Vitelliform Macular Dystrophy Macular Degeneration, Polymorphic Vitelline [decs.bvs.br]

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Neuronal Ceroid Lipofuscinosis Type 3

Abstract Three related patients from Colombia presented with a juvenile-onset neuronal ceroid lipofuscinosis. [neurology.org]

Batten disease is one of the most common of the NCLs with the classic juvenile onset of symptoms between ages 4 and 8 years. [ggc.org]

CLN3 is most commonly a juvenile-onset form of the disease. [flybase.org]

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X-linked Distal Spinal Muscular Atrophy Type 3

Highest motor milestone achieved ALL Characteristics Physical symptoms are similar to juvenile-onset spinal muscular atrophy, with the gradual onset of weakness, tremors [togetherinsma.com]

A collaborative study on the natural history of childhood and juvenile onset proximal spinal muscular atrophy (type II and III SMA): 569 patients. [cambridge.org]

Juvenile-onset, progressive with stabilisation after 2–4 years, affects primarily hands, very rare Finkel-type proximal spinal muscular atrophy (SMA-FK) 182980 VAPB 20q13.32 [ipfs.io]

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Young-Onset Parkinson Disease

To assess the prevalence, nature, and associated phenotypes of ATP13A2 gene mutations among patients with juvenile parkinsonism (onset 21 years) or young onset (between 21 [ncbi.nlm.nih.gov]

juvenile-onset parkinsonism (age at onset 20 years). [scielo.br]

Early onset Parkinson’s disease: are juvenile- and young-onset different? Mov. [futuremedicine.com]

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GM2-Gangliosidosis

We describe a 2-year-old black child with juvenile-onset disease, who presented with abnormal eye movements and cherry-red spots of the maculae. [ncbi.nlm.nih.gov]

26.2 and 34.7 months for the corresponding juvenile-onset variants. [ncbi.nlm.nih.gov]

Less severe, subacute (juvenile-onset) and chronic (adult-onset) variants are characterized by a broad spectrum of clinical manifestations and are associated with residual [ncbi.nlm.nih.gov]

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Amyotrophic Lateral Sclerosis Type 5

Juvenile ALS is more frequently familial in nature than the adult-onset forms. [atm.amegroups.com]

ALS5 is a juvenile-onset form of ALS and is inherited in an autosomal recessive manner. [symptoma.com]

Truncation mutations in SPG11 are associated with juvenile onset amyotrophic lateral sclerosis (ALS5), spastic paraplegia and other neurodegenerative conditions. [scholars.northwestern.edu]

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Neuronal Ceroid Lipofuscinosis Type 7

onset Signs and symptoms begin before 15 years of age 0003621 Mental deterioration Cognitive decline Cognitive decline, progressive Intellectual deterioration Progressive [rarediseases.info.nih.gov]

[…] limited to therapies that can help relieve some of the symptoms. 0000750 EEG abnormality 0002353 Generalized myoclonic seizures 0002123 Global developmental delay 0001263 Juvenile [rarediseases.info.nih.gov]

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Gangliosidosis GM1

People with type 2 who have late-infantile onset usually survive into mid-childhood, while those with juvenile onset may live into early adulthood. [rarediseases.info.nih.gov]

[…] initial scans, which were suggestive of T2-weighted signal intensity of the supratentorial WM, could be consistent with abnormal myelination observed in late infantile or juvenile-onset [movementdisorders.org]

Paramagnetic Signals in the Globus Pallidus as Late Radiographic Sign of Juvenile-Onset GM1 Gangliosidosis. Pediatr Neurol. 2014 Oct 16. [Medline]. [emedicine.com]

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Osteoporosis-Pseudoglioma Syndrome

Abstract Osteoporosis-pseudoglioma syndrome (OPPG) is a rare autosomal recessive syndrome characterized by juvenile-onset osteoporosis and ocular abnormalities due to a low-density [ncbi.nlm.nih.gov]

BACKGROUND: The osteoporosis-pseudoglioma syndrome is a rare autosomal recessive disorder characterized by severe juvenile-onset osteoporosis and congenital or early-onset [ncbi.nlm.nih.gov]

[…] blindness and severe juvenile-onset osteoporosis and spontaneous fractures OPPG ocular form of osteogenesis imperfecta Osteogenesis Imperfecta, Ocular Form Ops OSTEOPOROSIS-PSEUDOGLIOMA [wikidata.org]

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