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98 Possible Causes for Onset of Symptoms in First or Second Decade of Life, Pediatric Disorder

  • Erb Muscular Dystrophy

    The onset of symptoms usually occurs in the first or second decade of life. Affected individuals usually present with impairment of upper extremity elevation.[icd10data.com] Other neuromuscular disorders. Weinstein SL, Flynn JM, eds. Lovell and Winter's Pediatric Orthopaedics. 7th ed.[emedicine.medscape.com] Other neuromuscular disorders. Weinstein SL, Flynn JM, eds. Lovell and Winter's Pediatric Orthopaedics . 7th ed.[emedicine.medscape.com]

  • Hallervorden-Spatz Syndrome

    There is an early onset classic form with symptoms of extrapyramidal disease beginning in the first decade of life and rapid progression to loss of ambulation in about 15[disorders.eyes.arizona.edu] […] treatments and interventions Covers neurological, neuropsychiatric, and neuromedical disorders across the lifespan (pediatric, adult, and geriatric populations) Includes[books.google.com] Molecular & Medical Genetics, Pediatrics, and Neurology, Oregon Health & Science University, Portland, Oregon, USA Correspondence to Susan J.[journals.lww.com]

  • Facioscapulohumeral Muscular Dystrophy

    Symptoms Symptom onset usually occurs during the second decade of life, rarely in infancy or adulthood. Facial muscles are affect first.[symptoma.com] Complications of Neuromuscular Disorders. In Epp, Jr., CH & Bowen Jr., Complications in Pediatric Orthopaedic Surgery, 627-630,1995 Tachdjian M.O.[gait.aidi.udel.edu] Neuromuscul Disord. 2016 Jul;26(7):405-13. doi: 10.1016/j.nmd.2016.04.012. Epub 2016 Apr 22.[ncbi.nlm.nih.gov]

  • Hereditary Areflexic Dystasia

    Age of onset is in the second and third decades of life and rarely in the first. Recovery is usually complete and begins weeks to months after the onset of symptoms.[emedicine.medscape.com] National Organization for Rare Disorders (NORD). 2004; . Kleigman. Chapter 612 - Hereditary Motor-Sensory Neuropathies. Nelson Textbook of Pediatrics, 18th edition.[rarediseases.info.nih.gov]

  • Friedreich Ataxia

    Most affected people become wheelchair dependent by the second or third decade of life.[web.archive.org] Leigh syndrome (subacute necrotizing encephalomyopathy) is a rare, highly morbid and fatal pediatric disorder that results in severe neurological and neuromuscular dysfunction[bioelectron.com] […] searches, patients' associations, and National Centre for Rare Disorders.[ncbi.nlm.nih.gov]

  • Kearns-Sayre Syndrome

    Signs and symptoms [ edit ] Individuals with KSS present initially in a similar way to those with typical CPEO. Onset is in the first and second decades of life.[en.wikipedia.org] […] symptoms in infants, children, and young adults through images of common and unusual presenting features for over 300 pediatric disorders.[euro-libris.ro] The subject of numerous reports in the neuromuscular, genetic, and pediatric literature in recent years, very few cases of either disorder have ever been studied at autopsy[ncbi.nlm.nih.gov]

  • Hypertrophic Interstitial Neuropathy

    […] of symptoms usually in the second decade Progression is slower than in type 1 Nerve conduction studies are usually normal, but electromyography shows evidence of denervation[quizlet.com] Symptoms begin in first year of life Recessive transmission Hypotonia Muscular atrophy Weakness Ataxia Sensory disturbances Facial weakness and thick-lipped pouting mouth[quizlet.com] […] degree of abnormality on nerve conduction testing Autosomal Dominant Charcot-Marie-Tooth Type I or Hereditary Motor Sensory Neuropathy (HMSN) Autosomal dominant transmission Onset[quizlet.com]

  • Hypokalemic Periodic Paralysis

    […] is typically in the first or second decade of life (60% of cases have onset aged 16 years) with susceptible individuals experiencing sudden onset of perioral numbness; weakness[mdedge.com] The disorder has been described most frequently in Asian males.[pediatrics.aappublications.org] […] remission, onset in the first or second decade of life, and — for unknown reasons — amelioration at the age of 40 or 50.[doi.org]

  • Facial Hemiatrophy

    […] during the second decade of life.[en.wikipedia.org] The average age of onset is nine years of age, [2] and the majority of individuals experience symptoms before 20 years of age.[en.wikipedia.org] The disease has been reported to affect both sides of the face in 5-10% of the cases. [4] Symptoms and physical findings usually become apparent during the first or early[en.wikipedia.org]

  • Hyperkalemic Periodic Paralysis

    […] remission, onset in the first or second decade of life, and — for unknown reasons — amelioration at the age of 40 or 50.[doi.org] Swaiman's Pediatric Neurology: Principles and Practice. 6th ed. Philadelphia, PA: Elsevier; 2017:chap 151. Tilton AH. Acute neuromuscular diseases and disorders.[nlm.nih.gov] Pediatric Critical Care. 5th ed. Philadelphia, PA: Elsevier; 2017:chap 71. Text only[leehealth.org]

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