Create issue ticket

503 Possible Causes for Congenital Pain Insensitivity, Malabsorption Syndrome

  • 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[ncbi.nlm.nih.gov] 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] Abstract Hereditary sensory and autonomic neuropathy type IV (HSAN IV), or congenital insensitivity to pain with anhidrosis, is an autosomal recessive disorder characterized[ncbi.nlm.nih.gov]

  • Hypogammaglobulinemia

    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] Past medical history may also reveal secondary causes of hypogammaglobulinemia, such as nephrotic syndrome, malabsorption/gastroenteropathy (e.g., intestinal lymphangiectasia[online.epocrates.com] Other gastrointestinal diseases, such as sprue-like syndrome, ulcerative colitis, and Crohn disease, have been reported in patients with CVID and IgA deficiency.[emedicine.medscape.com]

  • Roy-Maroteaux-Kremp Syndrome

    […] dystrophy with cataracts and intellectual disability Congenital Pain Insensitivity Congenital Symmetric Circumferential Skin Creases Conn's syndrome Contiguous Abcd1/Dxs1375e[rgd.mcw.edu] Distichiasis Syndrome Lynch Lee Murday syndrome Lyngstadaas Syndrome Lysine Malabsorption Syndrome Maccario Mena Weir Syndrome MacDermot Winter Syndrome MacKay Shek Carr[rgd.mcw.edu] Muscular Dystrophy associated with Calf Hypertrophy, Microcephaly, and Severe Mental Retardation Congenital Muscular Dystrophy plus Mental Retardation congenital muscular[rgd.mcw.edu]

  • Intestinal Pseudo-Obstruction - Patent Ductus Arteriosus - Natal Teeth

    […] extreme pain disorder H00769 Hyperekplexia [PATH: hsa04080 ] H00774 Congenital insensitivity to pain H00775 Hemiplegic migraine [PATH: hsa04010 hsa04020 hsa04260 hsa04721[genome.jp] Congenital short femur * Congenital spherocytic anemia * Congenital spherocytic hemolytic anemia * Congenital stenosis of cervical medullary canal * Congenital sucrose isomaltose malabsorption[medicalgeek.com] [PATH: hsa04150 hsa04920 ] H01016 Primary bile acid malabsorption [PATH: hsa04976 ] H01023 Juvenile polyposis syndrome [PATH: hsa04060 hsa04350 hsa04110 hsa04310 hsa04520[genome.jp]

  • Tollner-Horst-Manzke Syndrome

    […] dystrophy with cataracts and intellectual disability Congenital Pain Insensitivity Congenital Symmetric Circumferential Skin Creases Conn's syndrome Contiguous Abcd1/Dxs1375e[rgd.mcw.edu] […] lipodystrophy type 4 Congenital heart block Congenital hydrocephalus Congenital hyperinsulinism Congenital insensitivity to pain Congenital insensitivity to pain with anhidrosis[rarediseases.info.nih.gov] Distichiasis Syndrome Lynch Lee Murday syndrome Lyngstadaas Syndrome Lysine Malabsorption Syndrome Maccario Mena Weir Syndrome MacDermot Winter Syndrome MacKay Shek Carr[rgd.mcw.edu]

  • Kashani-Strom-Utley Syndrome

    Anomalies/Mental Retardation Syndrome Congenital Pain Insensitivity congenital secretory sodium diarrhea 3 Conn's syndrome Contiguous Abcd1/Dxs1375e Deletion Syndrome Corneal[rgd.mcw.edu] Lynch Lee Murday syndrome Lyngstadaas Syndrome Lysine Malabsorption Syndrome Maccario Mena Weir Syndrome MacDermot Winter Syndrome MacKay Shek Carr Syndrome Macleod Fraser[rgd.mcw.edu] […] central hypoventilation syndrome Congenital Erythroderma with Palmoplantar Keratoderma, Hypotrichosis, and Hyper-IgE Congenital Hypoplastic Anemia with Multiple Congenital[rgd.mcw.edu]

  • Blue Diaper Syndrome

    […] adrenal hyperplasia Congenital adrenal hyperplasia due to 21-hydroxylase deficiency Congenital hepatic fibrosis Congenital ichthyosiform erythrodema Congenital insensitivity[akrabaevliligi.com] malabsorption syndrome (or “blue diaper syndrome”), and the methionine malabsorption syndrome (or “oasthouse urine disease”).[britannica.com] Bai JC: Malabsorption syndromes. Digestion 1998;59:530–546. Montalto M, Curigliano V, Santoro L: Management and treatment of lactose malabsorption.[karger.com]

  • Irritable Bowel Syndrome

    In another study, a different missense mutation (L811P) was found in two patients, one with congenital insensitivity to pain and the other with early-onset severe sensory[doi.org] Spectrum of malabsorption syndrome among adults & factors differentiating celiac disease & tropical malabsorption. Indian J. Med. Res. 136, 451–459 (2012). 76.[doi.org] syndromes Celiac disease Pancreatic insufficiency Endocrine disorders Hypothyroidism Hyperthyroidism Diabetes Addison's disease Endocrine tumors (very uncommon) Gastrinoma[aafp.org]

  • Kasznica-Carlson-Coppedge Syndrome

    […] dystrophy with cataracts and intellectual disability Congenital Pain Insensitivity Congenital Symmetric Circumferential Skin Creases Conn's syndrome Contiguous Abcd1/Dxs1375e[rgd.mcw.edu] Distichiasis Syndrome Lynch Lee Murday syndrome Lyngstadaas Syndrome Lysine Malabsorption Syndrome Maccario Mena Weir Syndrome MacDermot Winter Syndrome MacKay Shek Carr[rgd.mcw.edu] Muscular Dystrophy associated with Calf Hypertrophy, Microcephaly, and Severe Mental Retardation Congenital Muscular Dystrophy plus Mental Retardation congenital muscular[rgd.mcw.edu]

  • Davis-Lafer Syndrome

    […] dystrophy with cataracts and intellectual disability Congenital Pain Insensitivity Congenital Symmetric Circumferential Skin Creases Conn's syndrome Contiguous Abcd1/Dxs1375e[rgd.mcw.edu] Distichiasis Syndrome Lynch Lee Murday syndrome Lyngstadaas Syndrome Lysine Malabsorption Syndrome Maccario Mena Weir Syndrome MacDermot Winter Syndrome MacKay Shek Carr[rgd.mcw.edu] Muscular Dystrophy associated with Calf Hypertrophy, Microcephaly, and Severe Mental Retardation Congenital Muscular Dystrophy plus Mental Retardation congenital muscular[rgd.mcw.edu]

Further symptoms

Similar symptoms