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  2. Cutis marmorata telangiectatica congenita - Wikipedia

    en.wikipedia.org/wiki/Cutis_marmorata...

    Cutis marmorata telangiectatica congenita (CMTC) is a rare congenital vascular disorder that usually manifests in affecting the blood vessels of the skin. The condition was first recognized and described in 1922 by Cato van Lohuizen , [ 2 ] a Dutch pediatrician whose name was later adopted in the other common name used to describe the condition ...

  3. Macrocephaly-capillary malformation - Wikipedia

    en.wikipedia.org/wiki/Macrocephaly-capillary...

    This disorder was recognized as a distinct syndrome in 1997 and named macrocephaly-cutis marmorata telangiectasia congenita or M-CMTC. [12] [13] A new name, macrocephaly-capillary malformation, abbreviated M-CM, was recommended in 2007. [14] This new name was chosen to more accurately describe the skin markings associated with this disorder.

  4. Cutis marmorata - Wikipedia

    en.wikipedia.org/wiki/Cutis_marmorata

    Cutis marmorata (from Latin marmor, "marble") is a benign skin condition which, if persistent, occurs in Cornelia de Lange syndrome, trisomy 13 and trisomy 18 syndromes. [1] When a newborn infant is exposed to low environmental temperatures, an evanescent , lacy, reticulated red and/or blue cutaneous vascular pattern appears over most of the ...

  5. List of herbs with known adverse effects - Wikipedia

    en.wikipedia.org/wiki/List_of_herbs_with_known...

    Potentiates CNS sedatives, [3] chronic use might cause a reversible dry skin condition. [18] Khat: qat Catha edulis: Chronic liver dysfunction [3] [19] Kratom: Mitragyna speciosa: Hepatotoxicity [20] [19] Liquorice root Glycyrrhiza glabra: Hypokalemia, hypertension, arrhythmias, edema [5] Lobelia: asthma weed, pukeweed, vomit wort Lobelia inflata

  6. Hereditary hemorrhagic telangiectasia - Wikipedia

    en.wikipedia.org/wiki/Hereditary_hemorrhagic...

    Lesions lips, patient with hemorrhagic hereditary telangiectasia. Hereditary hemorrhagic telangiectasia (HHT), also known as Osler–Weber–Rendu disease and Osler–Weber–Rendu syndrome, is a rare autosomal dominant genetic disorder that leads to abnormal blood vessel formation in the skin, mucous membranes, and often in organs such as the lungs, liver, and brain.

  7. Marmorata - Wikipedia

    en.wikipedia.org/wiki/Marmorata

    Marmorata (from the Latin marmor for "marble") can refer to several different species or conditions presenting with a marbled appearance, including: Salmo marmoratus, marble trout; Acronicta marmorata, marble dagger moth; Synodontis marmorata, a catfish; Pleurodema marmorata, a frog; Cutis marmorata telangiectatica congenita, a disease

  8. Esophageal motility disorder - Wikipedia

    en.wikipedia.org/wiki/Esophageal_motility_disorder

    Compared to causes of mechanical obstruction, which usually coincide with difficulties only with solids, dysphagia occurs in both solid foods and liquids. Heartburn , odynophagia , chest pain , and dyspnea are frequent symptoms of esophageal motility disorders, as they are in other esophageal disorders .

  9. TEMPI syndrome - Wikipedia

    en.wikipedia.org/wiki/Tempi_syndrome

    Telangiectasia-erythrocytosis-monoclonal gammopathy-perinephric-fluid collections-intrapulmonary shunting syndrome TEMPI syndrome is an orphan disease where the patients share five characteristics from which the acronym is derived: telangiectasias , elevated erythropoietin and erythrocytosis , monoclonal gammopathy , perinephric fluid ...