Juvenile Onset: Causes & Reasons

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Possible Causes for Juvenile Onset

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]

Late-Onset Pompe Disease

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]

Juvenile Idiopathic Arthritis

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]

OBJECTIVE: To characterize the initial clinical and laboratory features of patients with systemic onset juvenile rheumatoid arthritis (soJRA) through a Web-based registry. [ncbi.nlm.nih.gov]

A | B | C | D | E | F | G | H | I | J | K | L | M | N | O | P | Q | R | S | T | U | V | W | X | Y | Z systemic onset juvenile rheumatoid arthritis a form of juvenile rheumatoid [web.archive.org]

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]

Systemic-Onset Juvenile Idiopathic Arthritis A definite diagnosis of systemic-onset JIA must await the development of arthritis. [emedicine.medscape.com]

[…] of polyarticular juvenile idiopathic arthritis (poly-JIA). [ncbi.nlm.nih.gov]

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]

Premature death is attributed to respiratory failure related to brain stem atrophy. [5] The minimal diagnostic criteria of Wolfram syndrome are juvenile-onset diabetes mellitus [neurologyindia.com]

Juvenile Primary Lateral Sclerosis

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

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

Background Mutations in the ALS2 gene cause juvenile-onset autosomal recessive amyotrophic lateral sclerosis (ALS) and hereditary spastic paraplegia. [jamanetwork.com]

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]

Hereditary Pheochromocytoma-Paraganglioma

Abstract Pheochromocytomas and paragangliomas are neuroendocrine tumors which arise from adrenal medulla, and sympathetic or parasympathetic nerves, respectively. Hereditary cases afflicted by both or either pheochromocytomas and paragangliomas have been reported: these are called hereditary[…] [ncbi.nlm.nih.gov]

Recurrent Respiratory Papillomatosis

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

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

Key words juvenile onset recurrent respiratory papillomatosis, bevacizumab, adjuvant therapy Introduction Juvenile-onset recurrent respiratory papillomatosis (JORRP) is a [oatext.com]

Juvenile Seronegative Polyarthritis

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]

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]

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]

Initial results from the national registry for juvenile-onset recurrent respiratory papillomatosis. RRP Task Force. [emedicine.medscape.com]

In the juvenile onset group more females were affected; in the adult onset group more males were affected. [ncbi.nlm.nih.gov]

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]

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]

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]

Juvenile Paralysis Agitans of Hunt

Do we know what causes juvenile-onset parkinson’s disease? There is a very strong genetic component to juvenile-onset parkinson’s disease. [scienceofparkinsons.com]

Early-onset cases that begin before age 20 are sometimes referred to as juvenile-onset Parkinson disease. [ Read More ] [icdlist.com]

Early-onset cases that begin before age 20 are sometimes referred to as juvenile-onset Parkinson disease. [Learn More] [icdlist.com]

Adult-Onset Still Disease

BACKGROUND: Anakinra treatment has been reported to be effective in some patients with systemic-onset juvenile idiopathic arthritis (SoJIA) or adult-onset Still disease (AoSD [ncbi.nlm.nih.gov]

[…] arthritis, and adult-onset rheumatoid arthritis) was performed. [ncbi.nlm.nih.gov]

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]

Systemic Juvenile Idiopathic Arthritis

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]

Juvenile onset Stills disease, also commonly described in literature as systemic-onset juvenile idiopathic arthritis (SoJIA), was initially established at the end of the 19th [symptoma.com]

Psoriatic Juvenile Idiopathic Arthritis

When we looked and compared the juvenile onset PsA group with the middle age 56 to 65 adult onset group similar disease characteristics were found as per table. [imedpub.com]

OBJECTIVE: To compare the patterns of joint involvement of patients with oligoarticular onset juvenile psoriatic arthritis (Oligo-JPsA) and pauciarticular onset juvenile rheumatoid [ncbi.nlm.nih.gov]

— Juvenile Idiopathic Arthritis — Idiopathic Arthritis, Juvenile — Juvenile-Onset Still Disease — Juvenile Onset Still Disease — Still's Disease, Juvenile-Onset — Juvenile-Onset [mesh.kib.ki.se]

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]

This is called "juvenile onset" Huntington's Disease. [huntingtonsnsw.org.au]

Childhood-onset (Juvenile) Huntington's disease: A rare case report. [pediatricneurosciences.com]

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]

[…] medical disorder Alternative Titles: IDDM, juvenile-onset diabetes, type 1 diabetes, type 1 diabetes mellitus, type I diabetes, type I diabetes mellitus Learn about this topic [britannica.com]

Explore these free sample topics: -- The first section of this topic is shown below -- Classification Diabetes is classified as type 1 (formerly called juvenile-onset or insulin-dependent [hopkinsguides.com]

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 [cambridge.org]

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]

Esophoria

Goss D (1991) Clinical accommodation and heterophoria findings preceding juvenile onset of myopia. Optom Vis Sci 68:110–116 PubMed CrossRef Google Scholar 4. [link.springer.com]

Pacella, R. et al. (1999). " Role of Genetic Factors in the Etiology of Juvenile-Onset Myopia Based on a Longitudinal Study of Refractive Error, " Optometry and Vision Science [patents.google.com]

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]

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

Distal Spinal Muscular Atrophy Type 5

7q34–q36 Autosomal dominant Autosomal dominant juvenile distal spinal muscular atrophy Juvenile onset DHMN2A 158590 HSPB8 12q24.23 Autosomal dominant Autosomal dominant distal [en.wikipedia.org]

The second juvenile-onset form of ALS is ALS 4, an autosomal-dominantly inherited distal motor neuronopathy with pyramidal symptoms [ Chance et al., 1998 ]. [clinicalgate.com]

SCN9A Dysautonomia, FRRS1L-related FRRS1L Dyskinesia, familial, with facial myokymia ADCY5 Dyslexia PCDH11X Dyssegmental dysplasia, Silverman-Handmaker type HSPG2 Dystonia juvenile-onset [centogene.com]

Pompe Disease

Abstract The authors describe two novel mutations of the acid alpha-glucosidase gene, P361L and R437C, which define the juvenile-onset glycogen storage disease type II (GSDII [neurology.org]

At juvenile onset, a more moderate vacuolization without significant differences in overall morphology is notable. [ncbi.nlm.nih.gov]

[…] dyspnea Orthopnea Sleep apnea Hyperlordosis and/or scoliosis (childhood and juvenile onset) Hepatomegaly (childhood and juvenile onset) Macroglossia (childhood onset) Difficulty [centogene.com]

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]

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]

[…] are employed in juvenile and adult onset SpA. [ard.bmj.com]

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

Huntington Disease-Like Type 3

Unlike Juvenile onset HD, seizures and eye movement abnormalities are usually not described. [hopkinsmedicine.org]

Successive generations tend to have earlier onset Juvenile onset symptoms Clumsiness Hyperreflexia Occulomotor disturbances Physical instability/falls Rigidity Mental deterioration [arupconsult.com]

Syndrome Information Clinical Description Huntington Disease-like 2 (HDL2) is clinically similar to Juvenile onset Huntington Disease. [hopkinsmedicine.org]