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934 Possible Causes for Congenital Pain Insensitivity, Intestinal Hypomotility

  • Autonomic Neuropathy

    Abstract Congenital insensitivity (HSAN) to pain is a rare disorder, which affects the body's painprotective mechanism and predisposes the patient to increased risk and incidence[] 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[] Abstract Hereditary sensory and autonomic neuropathy type IV (HSAN IV), or congenital insensitivity to pain with anhidrosis, is an autosomal recessive disorder characterized[]

  • Channelopathy-Associated Congenital Insensitivity to Pain

    Consider performing sequence analysis of: SCN11A first in a newborn with severe intestinal hypomotility.[] Congenital pain insensitivity is a rare genetic disorder characterized by the inability to perceive pain.[] Abstract The congenital pain insensitivity syndrome is accompanied by: a) the presence of a yellow-brown pigment in the basal layer of the epidermis with the histochemical[]

  • Colonic Pseudo-Obstruction

    We suggest prescribers should exercise caution when prescribing trihexyphenidyl in patients with long-term intestinal hypomotility issues.[] K59.8 Hypofunction intestinal K59.8 Hypomotility intestine K59.8 Ileus (bowel) (colon) (inhibitory) (intestine) K56.7 ICD-10-CM Diagnosis Code K56.7 Ileus, unspecified 2016[] K59.8 Hyperemia (acute) (passive) R68.89 ICD-10-CM Diagnosis Code R68.89 Other general symptoms and signs 2016 2017 2018 2019 Billable/Specific Code enteric K59.8 intestine[]

    Missing: Congenital Pain Insensitivity
  • Intestinal Pseudo-Obstruction

    Yan JK 1, 2, 3 , Zhou KJ 1, 2, 3 , Huang JH 1 , Wu QQ 1 , Zhang T 1 , Wang CC 4 , Cai W 5, 6, 7 . Author information 1 Department of Pediatric Surgery, Xin Hua Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, 1665 Kongjiang Rd, Shanghai, 200092, China. 2 Shanghai Institute for Pediatric Research,[…][]

    Missing: Congenital Pain Insensitivity
  • Intestinal Hypomotility

    OBJECTIVE: Small intestinal hypomotility is an important cause of small intestinal bacterial overgrowth, yet assessment of small intestinal motility in this setting is problematic[] Abstract Dilatation of unobstructed extrahepatic bile ducts was observed in patients with conditions associated with intestinal hypomotility.[] CONCLUSION: Epidural naloxone reduces epidural morphine-induced intestinal hypomotility without reversing its analgesic effects.[]

    Missing: Congenital Pain Insensitivity
  • Amyloidosis

    Amyloidosis a rare disorder characterised by the deposition of amyloid protein aggregates in different organ systems throughout the body with resulting functional impairment of affected organs. It can present with localised or multisystemic deposits. Diagnosis is often delayed due to the non-specific nature of the[…][]

    Missing: Congenital Pain Insensitivity
  • Systemic Amyloidosis

    Persistent pleural effusions (PPE) occur in 1-2% of cases of systemic amyloidosis and have been postulated to result from direct disruption of the pleura by amyloid deposits. Patients are typically treated with percutaneous pleural drainage techniques. Pleural biopsies, done most commonly via percutaneous[…][]

    Missing: Congenital Pain Insensitivity
  • Hypermagnesemia

    hypomotility.[] Intestinal hypomotility causes decreased elimination of the mineral as well as its increased absorption from the gastrointestinal tract.[] hypomotility due to narcotics and anticholinergics or bowel obstruction and chronic constipation Lithium intoxication Rhabdomyolysis Tumor lysis syndrome Advanced age Pregnancy[]

    Missing: Congenital Pain Insensitivity
  • Hereditary Sensory Neuropathy

    See Congenital Insensitivity to Pain Overview.[] From Wikidata Jump to navigation Jump to search congenital disorder of nervous system Hereditary sensory and autonomic neuropathy (disorder) congenital insensitivity to pain[] Entry H00265 Disease Name Hereditary sensory and autonomic neuropathy Subgroup Familial dysautonomia [DS: H01987 ] Congenital pain insensitivity with anhidrosis [DS: H01836[]

    Missing: Intestinal Hypomotility
  • Autosomal Dominant Hereditary Sensory and Autonomic Neuropathy

    For example: HSAN2D (channelopathy-associated congenital insensitivity to pain) : patients have homozygous mutations in the SCN9A gene 4,7.[] Keywords: Congenital analgesia, congenital insensitivity to pain with anhidrosis, familial trophoneurosis, hereditary sensory and autonomic neuropathy, hereditary sensory[] Nagasako EM, Oaklander AL, Dworkin RH - Congenital insensitivity to pain: an update. Pain, 2003;101:213-219. [ Links ] 16.[]

    Missing: Intestinal Hypomotility

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