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674 Possible Causes for Hypomyelination, Loss of Appetite

  • Anemia

    McGregor, do you want to bring up the protein-energy malnutrition literature and hypomyelination? Dr.[web.archive.org] Nausea, vomiting, and loss of appetite. Nausea and vomiting and loss of appetite may cause a lack of nutrients. The body needs these nutrients to make red blood cells.[cancer.net] Symptoms that may occur first include: Feeling weak or tired more often than usual, or with exercise Headaches Problems concentrating or thinking Irritability Loss of appetite[medlineplus.gov]

  • Leukodystrophy

    Hypomyelinating leukodystrophies are genetic disorders characterized by insufficient myelin deposition during development.[ncbi.nlm.nih.gov] Imagine your child experiencing an unexplained sudden loss of basic functions – a toddler who once constantly walked and ran suddenly stumbling with each step; an infant with[myelin.org] […] in POLR3A encoding the largest subunit of RNA polymerase III (Pol III) were found to be responsible for the majority of cases presenting with three clinically overlapping hypomyelinating[ncbi.nlm.nih.gov]

  • Leigh's Disease

    The findings suggest that there is hypomyelination of peripheral nerves leading eventually to demyelination.[ncbi.nlm.nih.gov] Symptoms usually begin between ages of three months and two years and include loss of appetite, vomiting, irritability and seizure activity.[wikidata.org] The earliest signs may be poor sucking ability,and the loss of head control and motor skills.These symptoms may be accompanied by loss of appetite, vomiting, irritability,[ninds.nih.gov]

  • Neonatal Adrenoleukodystrophy

    (CACH) Childhood Ataxia with Diffuse CNS Hypomyelination (CACH or Vanishing White Matter Disease) Craniometaphysical Dysplasia with Leukoencephalopathy Cystic Leukoencephalopathy[huntershope.org] The adrenal glands in patients with ALD often produce insufficient amounts of cortisol, which may lead to muscle weakness and fatigue, weight loss and decreased appetite,[healthinhandorganics.com] Childhood ataxia with cerebral hypomyelination Childhood ataxia with cerebral hypomyelination (CACH), also known as vanishing white matter disease (VWMD), is an autosomal[rarediseases.org]

  • Déjerine-Sottas Disease

    , consistent with congenital hypomyelination neuropathy (CHN).[ncbi.nlm.nih.gov] Avoid with a history of seizures, bleeding disorders, eating disorders (such as anorexia or bulimia), or anemia (low levels of iron). Avoid if pregnant or breastfeeding.[lindbergnutrition.com] They include Charcot-Marie-Tooth disease, Dejerine-Sottas disease, congenital hypomyelinating neuropathy and hereditary neuropathy with liability to pressure palsy.[ncbi.nlm.nih.gov]

  • Arthritis

    Stowe and Lakshmi Raman, Perinatal chronic hypoxia induces cortical inflammation, hypomyelination, and peripheral myelin‐specific T cell autoreactivity, Journal of Leukocyte[doi.org] Loss of appetite. Inflammation of the eye. Difficulty with daily living activities such as walking, dressing, and playing.[cdc.gov] Loss of appetite. What causes RA? RA is a form of arthritis and a type of autoimmune disease. It occurs when the body’s immune system attacks its own joint tissue.[familydoctor.org]

  • Hirschsprung's Disease

    Neurologic studies disclosed brain hypomyelination, peripheral dysmyelinating neuropathy, and enteric neuroglia deficiency, which exclusively implied systemic glial maldevelopment[ncbi.nlm.nih.gov] […] of appetite Cleveland Clinic is a non-profit academic medical center.[my.clevelandclinic.org] Peripheral neuropathy with hypomyelination, chronic intestinal pseudo- obstruction and deafness: a developmental "neural crest syndrome" related to a SOX10 mutation.[ncbi.nlm.nih.gov]

  • Microcephalic Primordial Dwarfism due to ZNF335 Deficiency

    Cataract Syndrome Leukodystrophy , Hypomyelinating, 5 Madras Motor Neuron Disease Mast Syndrome Microcephalic Primordial Dwarfism Due To Znf335 Deficiency Orofaciodigital[familydiagnosis.com] Angelman syndrome-like, 105830 SERPING1 Angioedema, hereditary, types I and II, 106100 MEN1 Angiofibroma, somatic PAX6 Aniridia, 106210 RSPO4 Anonychia congenita,206800 BDNF Anorexia[gsdseq.ir] Obsessive-compulsive disorder, protection against} 164230 113505 Autosomal dominant BDNF 11p14.1 Central hypoventilation syndrome, congenital 209880 113505 Autosomal dominant BDNF 11p14.1 {Anorexia[mnglabs.com]

  • Pyruvate Carboxylase Deficiency

    Anatomic-pathologic studies revealed periventricular cysts and diffuse hypomyelination. Prenatal diagnosis of a further sibling was performed.[ncbi.nlm.nih.gov] The signs and symptoms may include: Developmental delays and mental retardation Poor feeding, loss of appetite Lethargy and fatigue Seizures, neonatal fits Abdominal pain[dovemed.com] Hypomyelination, cystic lesions, and gliosis of the cortex or cerebellum with gray matter degeneration or necrotizing encephalopathy occur in some infants.[emedicine.com]

  • Kallmann Syndrome Type 4

    Other names for 4H syndrome: Ataxia, Hypodontia and Hypomyelination (AHH) Ataxia, delayed dentition and Hypomyelination (ADD) Pol III – related Leukodystrophy[leukodystrophyresourceresearch.org] […] of weight due to dietary restriction, the loss of weight and of appetite being less extreme than in anorexia nervosa and unassociated with psychological problems. hypogonadotropic[medical-dictionary.thefreedictionary.com] Anorexia nervosa commonly results in functional hypogonadotropic hypogonadism.[depts.washington.edu]

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