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700 Possible Causes for Hypomyelination, Hypotension

  • Anemia

    McGregor, do you want to bring up the protein-energy malnutrition literature and hypomyelination? Dr.[] HBO was discontinued in the survivors when they no longer suffered from hypoxic sprue, postural hypotension, and usually when the Hct was 22% or greater and the Hb was 7 g[] Hypovolemia leads to hypotension, which is detected by stretch receptors in the carotid bulb, aortic arch, heart, and lungs.[]

  • Aromatic L-Amino Acid Decarboxylase Deficiency

    Of 15 MR examinations, the major changes included 6 (40%) with diffusely prominent bilateral frontal sulci, 10 (67%) with prominent frontal horns, and 12 (80%) with hypomyelination[] […] aromatic L-amino acid decarboxylase deficiency who developed serious cardiac rhythm disturbances during treatment with intravenous dopamine and norepinephrine for severe hypotension[] […] constriction of the pupils of the eyes (miosis), inappropriate or impaired sweating, nasal congestion, drooling, reduced ability to control body temperature, low blood pressure (hypotension[]

  • Leukodystrophy

    […] 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[] Urinary and rectal incontinence, orthostatic hypotension, and progressive spasticity are the main symptoms.[] […] and sixth decades (mean age of 40 years) of life with early presentation of autonomic symptoms, including bowel/bladder dysfunction, impotence in males, and orthostatic hypotension[]

  • Dysautonomia

    : Neuropathies Sensory ataxia, Dominant SPG8 Triglycerides Tuberculosis Vasculitis: Treatment Oct 2006 Coenzyme Q 10 deficiency COQ2 PDSS2 Fukutin Cardiomyopathy LGMD 2L Hypomyelination[] […] with postprandial hypotension when oral foods and fluids are withheld perioperatively.[] […] absence of the vas deferens Congenital Cataracts, Facial Dysmorphism, and Neuropathy Congenital central hypoventilation Congenital ectodermal dysplasia of face Congenital hypomyelinating[]

  • Methylmalonic Acidemia

    Postmortem examination disclosed marked brain atrophy with old lesions of hypomyelination, granule cell reduction, and spongy changes scattered in the cerebral cortex, white[]

  • Pelizaeus-Merzbacher Disease

    Hypomyelinating leukoencephalopathy is a heterogeneous disorder caused by mutations in several-different genes.[] Urinary and rectal incontinence, orthostatic hypotension, and progressive spasticity are the main symptoms.[] A diffuse pattern of hypomyelination is seen on magnetic resonance imaging (MRI) of PMD/SPG2 patients.[]

  • Dopamine Beta-Hydroxylase Deficiency

    […] deficiency D-2-hydroxyglutaric aciduria D-bifunctional protein deficiency D-glycericacidemia Danon disease DCMA syndrome DDOST-CDG (CDG-Ir) Deafness, dystonia, and cerebral hypomyelination[] With a dose of 500 mg twice daily by mouth, blood pressure rose gradually from 100/55 to 145/85 mm Hg, and orthostatic hypotension disappeared.[] During chronic treatment supine blood pressure rose from 100-115/55-65 to 140-145/80-85 mmHg and orthostatic hypotension disappeared.[]

  • Periventricular Leukomalacia

    At P7, apoptosis and hypomyelination in periventricular white matter were evaluated by immunohistochemical assessments.[] […] and multivariate logistic regression analysis as independent risk factors: birth weight (odds ratio, 4.31; 95% confidence interval, 1.54-12.06; P 0.005), early neonatal hypotension[] Hypotension: Abnormally low blood pressure. Hypoxemia: Abnormally low concentration of oxygen in the blood.[]

  • Roy-Maroteaux-Kremp Syndrome

    MICROCEPHALY, ATAXIA, AND SEIZURES NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, EPILEPSY, AND BRAIN ATROPHY Neurodevelopmental Disorder with Microcephaly, Epilepsy, and Hypomyelination[] Sudden Unexpected Nocturnal Death Syndrome Summitt Syndrome SUNCT Syndrome superior mesenteric artery syndrome Superior Vena Cava Syndrome Supernumerary Der(22)t(8 supine hypotensive[]

  • Autosomal Recessive Primary Microcephaly Type 10

    Cataract Syndrome Leukodystrophy , Hypomyelinating, 5 Madras Motor Neuron Disease Mast Syndrome Microcephalic Primordial Dwarfism Due To Znf335 Deficiency Orofaciodigital[] KIF3A TRP53 Hypertrophy ANGPT1 EDN1 Osteochondrodysplasias DLL3 VEGFA Left Ventricular Hypertrophy EDN1 MYC Abnormalities, Multiple CTNNB1 FGFR2 Cecal Neoplasms CTNNB1 TRP53 Hypotension[] Hypomyelination with atrophy of the basal ganglia and cerebellum (H-ABC) is a rare hypomyelinating leukodystrophy characterized by infantile or childhood onset of motor developmental[]

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