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15 Possible Causes for Jaundice, Telangiectasia on Lips and Oral Mucosa

  • Hereditary Hemorrhagic Telangiectasia

    Evaluations of her jaundice revealed chronic parenchymal liver disease with multiple nodules in the liver with early portal hypertension.[] Diagnosis HHT is a clinical diagnosis based on four features: Spontaneous, recurrent nosebleeds Telangiectasias of the lips, oral mucosa (inside the mouth), tongue, fingertips[] Liver AVMs may be suspected because of abnormal liver function tests in the blood, because the symptoms of heart failure develop, or because of jaundice or other symptoms[]

  • Iron Deficiency

    WHO recommends delayed cord clamping but mentions the risk for polycythemia and neonatal jaundice ( Table 1 ). 41 However, a recent RCT found that clamping before administration[] Pigmentation of the lips and oral mucosa, which may suggest Peutz-Jeghers syndrome.[] Multiple telangiectasias, which may be a feature of hereditary haemorrhagic telangiectasia, also known as Osler-Weber-Rendu syndrome .[]

  • Coagulation Abnormalities

    In patients with obstructive jaundice, bile salts, which are necessary for the emulsification and absorption of the fat-soluble vitamins (vitamins A, D, E, and K), cannot[] People with this disorder have small red-to-violet telangiectatic lesions on the face, lips, oral and nasal mucosa, and tips of the fingers and toes.[] The criteria used for the diagnosis of CLD were based on: Presence of cardinal signs and symptoms including ascites, hepatomegaly, splenomegaly, jaundice, palmar erythema,[]

  • Microcytic Anemia

    […] it: AAMIF Aplastic Anemia and MDS International Foundation Community » Non-Profit Organizations Rate it: ABLA Acute Blood Loss Anemia Medical » Physiology Rate it: JACCOL Jaundice[] Pigmentation of the lips and oral mucosa, which may suggest Peutz-Jeghers syndrome.[] -No jaundice or other signs of hemolysis.[]

  • Hemoptysis

    Accompanying symptoms fever, chest pain, coughing, purulent sputum, mucocutaneous bleeding, jaundice.[] Telangiectasia, especially on the lips or buccal mucosa, may raise the diagnosis of hereditary hemorrhagic telangiectasia.[] Oral or genital ulcerations may be the initial presentation of a Beçhet disease. Calf tenderness may suggest the diagnosis of pulmonary embolism.[]

  • Jejunal Vascular Anomaly with Hemorrhage

    Flatulence • Palliative resection -Dyspepsia • Palliative bypassLate signs - LOW -anemia -dysphagia -vomiting -epigastric/back pain - epigastric mass -sign of metastases (jaundice[] Characteristic Mucocutaneous Telangiectasia Pictures and Photos of Hereditary Hemorrhagic Telangiectasias on his ears, face, lips, tongue, and oral and nasal mucosa.[] Other clinical signs are more exceptional: jaundice by pancreatobiliary reflux secondary to clot formation [ 1 et 2 ] , vomiting, weight loss, palpable pulsating epigastric[]

  • Telangiectasia Macularis Eruptiva Perstans

    Prolonged obstructive jaundice and haemangiomas: report of 2 cases. Arch Dis Child 1974;49:665-7. 73. Mclean RH, Moller JH, Warwick WJ.[] Similarly, telangiectasia mainly over the lips and oral mucosa and sometimes on the face and dorsum of the hands in association with a nosebleed are seen in HHT.[] Other complications have included the Kasabach-Merritt syndrome, 4,64,80-82 convulsions, 64 intestinal haemorrhage 60 and obstructive jaundice. 68,72 Certain investigations[]

  • Hereditary Koilonychia

    Patient presents with chipmunk facies, jaundice, and splenomegaly. Before doing other tests, what disease do you suspect?[] Pigmentation of the lips and oral mucosa, which may suggest Peutz-Jeghers syndrome.[] Jaundice, abdo pain Neuro eg. Headache, seizures, weakness, sensory loss, speech, vision GU eg. Haematuria PMH eg. hypertension Dx- any blood thinners? Iron tablets?[]

  • X-Linked Mandibulofacial Dysostosis

    Moderate to severe macrocytic anemia presenting occasionally in utero as severe anemia associated with hydrops fetalis but more commonly in neonates as hepatomegaly, early jaundice[] Mucosa Isolated cleft palate and cleft lip with or without cleft palate, Hereditary hemorrhagic telangiectasia, Multiple mucosal neuroma syndrome, Neurofibromatosis of von[] , repeated infections, and periodic episodes of pain 1/1,00,000 1/500 African Americans 1/1,000 Hispanic Americans Early childhood Spherocytosis ANK1, SPTB, SPTA1, EPB42 Jaundice[]

  • Oculocerebral Hypopigmentation Syndrome Type Cross

    18pter-p11.2, ferrochelatase deficiency; onset 1-4 years old. early; burning erythematous plaques in sun distribution. late; waxy thickened scarring with cholelithiasis, jaundice[] , and oral mucosa.[] Telangiectasia may occur.[]

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