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749 Possible Causes for Congenital Pain Insensitivity, Pediatric Disorder

  • Channelopathy-Associated Congenital Insensitivity to Pain

    Congenital pain insensitivity is a rare genetic disorder characterized by the inability to perceive pain.[symptoma.com] This case report highlights the rare association of congenital insensitivity to pain and anhidrosis with seizure disorder.[content.iospress.com] J Pediatr Neurosci 2012;7:156-7 Dear Sir, Congenital insensitivity to pain with anhidrosis (CIPA) or hereditary sensory; Type IV autonomic neuropathy, is an extremely rare[pediatricneurosciences.com]

  • Juvenile Polyp

    insensitivity to pain with anhidrosis ) KIT ( KIT Piebaldism, Gastrointestinal stromal tumor ) STPK AMHR2 ( Persistent Müllerian duct syndrome II ) TGF beta receptors : Endoglin[en.wikipedia.org] Wireless capsule endoscopy for oscure small-bowel disorders: Final results of the first pediatric controlled trial . Clin Gastroenterol Hepatol 2005; 3 :264–270. 21.[nature.com] Older paternal age and fresh gene mutation: data on additional disorders. J Pediatr . 1975 Jan. 86(1):84-8. [Medline] .[emedicine.medscape.com]

  • Familial Dysautonomia

    1型遺伝性感覚性自律神経性ニューロパチー 4型遺伝性感覚性自律神経性ニューロパチー Autosomal Dominant Neuropathy Hereditary Sensory Radicular Congenital Insensitivity to Pain with Anhidrosis Congenital Pain Insensitivity[lsd-project.jp] […] autonomic neuropathies (HSAN) and for other pediatric disorders with autonomic dysfunction.[web.archive.org] disorders with induced pluripotent stem cells Matthew D.[nature.com]

  • Rasmussen Syndrome

    先天性無痛無汗症 Congenital insensitivity to pain with anhidrosis 無痛無汗症 1 不要 HPS1076 HPS1077 Congenital insensitivity to pain with anhidrosis (CIPA), unknown genetic etiology 先天性無痛無汗症[cell.brc.riken.jp] Recognition of the syndrome, especially in pediatric populations, is difficult and often undiagnosed and/or confused with neurological disorders with similar clinical features[ncbi.nlm.nih.gov] […] work in the neurosciences, genetics, electroencephalography, pediatric and adult neurology, neuropharmacology, neurosurgery, and psychiatry.[books.google.ro]

  • Pseudopseudohypoparathyroidism

    insensitivity to pain with anhidrosis ) KIT ( KIT Piebaldism, Gastrointestinal stromal tumor ) STPK AMHR2 ( Persistent Müllerian duct syndrome II ) TGF beta receptors : Endoglin[en.wikipedia.org] Germany J Pediatr 150:618-22, 622.e1-5. 2007 ..To analyze the frequencies and clinical presentation of definable somatic disorders in children who are overweight...[labome.org] Abstract Patients with Albright hereditary osteodystrophy (AHO) phenotype are usually seen in pediatric endocrinology policlinics when they are evaluated for short stature[degruyter.com]

  • Kallmann Syndrome

    insensitivity to pain with anhidrosis ) KIT ( KIT Piebaldism, Gastrointestinal stromal tumor ) STPK AMHR2 ( Persistent Müllerian duct syndrome II ) TGF beta receptors : Endoglin[en.wikipedia.org] Developmental disorders with olfactory abnormalities, developmental lag, heart malformations, external genital malformations.[ncbi.nlm.nih.gov] Michael Freemark, Obesity and the Endocrine System, Part I: Pathogenesis of Weight Gain in Endocrine and Metabolic Disorders, Pediatric Obesity, 10.1007/978-3-319-68192-4_[doi.org]

  • Hemophilic Arthropathy

    insensitivity to pain.[physio-pedia.com] John Akabutu Comprehensice Centre for Bleeding DisordersPediatric Division Stollery Children’s Hospital Clinic Director Dr.[hemophilia.ca] Montgomery hereditary clotting factor deficiencies (bleeding disorders).[err.eg.net]

  • Epidermolysis Bullosa

    insensitivity to pain with anhidrosis ) KIT ( KIT Piebaldism, Gastrointestinal stromal tumor ) STPK AMHR2 ( Persistent Müllerian duct syndrome II ) TGF beta receptors : Endoglin[en.wikipedia.org] Bullous disorders of childhood. In: Hurwitz Clinical Pediatric Dermatology: A Textbook of Skin Disorders of Childhood and Adolescence. 5th ed.[mayoclinic.org] Abstract Epidermolysis bullosa is a group of rare genetic disorders with multiple organ system involvement.[ncbi.nlm.nih.gov]

  • Paramyotonia Congenita

    Fast Channel Myasthenic Syndrome Chain403 Congenital Fast-channel Myasthenic Syndrome Chain407 Congenital Insensitivity to Pain Syndrome Chain500 Delayed Sleep Phase Syndrome[sequencing.com] Kang, The Spectrum of Myotonic and Myopathic Disorders in a Pediatric Electromyography Laboratory Over 12 Years, Pediatric Neurology, 47, 2, (97), (2012).[doi.org] - Current Pediatric Research (2010) Volume 14, Issue 1 Paramyotonia Congenita is a rare neuromuscular disorder characterized by paradoxical myotonia.[alliedacademies.org]

  • Tibia Varum

    Congenital insensitivity to pain Congenital insensitivity (indifference) to pain is a rare syndrome inherited as an autosomal recessive trait.[clinicalgate.com] 12/18/2017 by Megan Young, MD, Children’s National Medical Center, Washington, DC Pediatric Lower Extremity Disorders Topics covered in this section: Genu varum Physiologic[posna.org] […] you need to effectively diagnose and treat pediatric musculoskeletal disorders.[books.google.ro]

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