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203 Possible Causes for Coarse Facial Features, Coronary Artery Disease, Osteopenia and Osteoporosis

  • Fabry Disease

    , ventricular tachycardia, atrial fibrillation and coronary artery disease).[ncbi.nlm.nih.gov] Often patients have slight builds with characteristic coarse facial features and delayed puberty.[patient.info] Osteopenia and osteoporosis: previously unrecognized manifestations of Fabry disease. Clin Genet 2005; 68 : 93–95. 81 Schiffmann R, Murray GJ, Treco D, Daniel P, et al.[nature.com]

  • Chronic Alcoholism

    […] hypertension Apoplexy Coronary heart disease Metabolism : Hypertriglyceridemia Hyperuricemia Hypoglycemia Porphyria cutanea tarda Hyperchromic anemia in folic acid deficiency[flexikon.doccheck.com] Heart attacks and angina [chest pain] are the most common results of coronary heart disease. Someone has a heart attack when their coronary arteries become blocked.[drinkaware.co.uk] Zieveâ s syndrome Pancreas : Acute pancreatitis Chronic calcifying pancreatitis Cardiovascular system: Holiday heart syndromes Dilatative cardiomyopathy caused by alcoholism Arterial[flexikon.doccheck.com]

  • Mucopolysaccharidosis

    Severe coronary artery disease is well recognized in severe type I mucopolysaccharidosis (Hurler syndrome), but unexpected coronary artery disease occurs in other, "non-Hurler[ncbi.nlm.nih.gov] facial features, developmental delay, and an elevated quantitative urine glycosaminoglycan (GAG) level.[ncbi.nlm.nih.gov] The patient presented with mild coarse facial features, short stature, mild dyspnea, sternal protrusion, mild lumbar hyperlordosis, and waddling gait owing to bilateral femoral[ncbi.nlm.nih.gov]

  • Mucopolysaccharidosis 2

    A thickened myocardium eventually leads to coronary artery compromise, myocardial disease, and, in conjunction with airway disease, pulmonary hypertension.[emedicine.medscape.com] Other symptoms may include carpal tunnel syndrome, coarse facial features, deafness, hairy body (hypertrichosis), joint stiffness, and a large head (macrocephaly).[secure.ssa.gov] There are some obvious physical signs of Hunter syndrome, such as coarse facial features and an enlarged liver and spleen, as well as some less noticeable symptoms. 2 Symptoms[rare2aware.com]

  • Old Age

    To evaluate the use of percutaneous transluminal coronary angioplasty (PTCA) in elderly coronary artery disease (CAD) patients.[ncbi.nlm.nih.gov] These scores don’t mean you will progress from osteopenia to osteoporosis or experience a fracture. Instead, they encourage prevention methods.[healthline.com] Abstract Objective To evaluate the use of percutaneous transluminal coronary angioplasty (PTCA) in elderly coronary artery disease (CAD) patients.[doi.org]

  • Adrenocortical Carcinoma

    He reported no chest symptom and did not exhibit any established risk factors for coronary artery disease, such as diabetes, obesity, hypertension or relevant family history[ncbi.nlm.nih.gov] , diabetes, history of hypertension, elevated LDL, first degree relative with coronary artery disease) will undergo full cardiac evaluation and will not be eligible if they[clinicaltrials.gov] History of congestive heart failure and/or an LVEF less than 40% Note: Patients at increased risk for coronary artery disease or cardiac dysfunction (e.g., greater than 65yo[clinicaltrials.gov]

  • Costello Syndrome

    The most likely diagnosis is: a) Coronary artery disease b) Dilated cardiomyopathy c) Hypertrophic cardiomyopathy 3) In this paper not much detailed information is given about[aadmd.org] facial features and skeletal and cardiac abnormalities.[ncbi.nlm.nih.gov] Other characteristics of special note were hip dysplasia (45%), foot deformities requiring surgical intervention (38%) and osteopenia/osteoporosis (47%).[ncbi.nlm.nih.gov]

  • Winchester Syndrome

    […] sclerosis of infancy , see generalized arterial calcification of infancy median facial cleft syndrome , see frontonasal dysplasia Mediterranean anemia , see beta thalassemia[herenciageneticayenfermedad.blogspot.com] Affiliated tissues include bone , skin and testes , and related phenotypes are gingival overgrowth and coarse facial features OMIM : 57 Winchester syndrome presents with severe[malacards.org] osteopenia / demineralisation / osteomalacia / rickets - Restricted joint mobility / joint stiffness / ankylosis - Short stature / dwarfism / nanism - Tarsal anomaly [csbg.cnb.csic.es]

  • Simpson Dysmorphia Syndrome

    Dry ice used to keep food cold, pyrethroid Pesticides Pre-existing illness—such as anemia, asthma, COPD, and coronary arterial disease—the stresses of flight could exacerbate[wikivisually.com] facial features, widely spaced eyes, a short nose with anteverted nares, gingival overgrowth, a wide mouth, short limbs with short distal phalanges, and a small penis.[zora.uzh.ch] […] disability-sparse hair syndrome Osteopenia-myopia-hearing loss-intellectual disability-facial dysmorphism syndrome Osteoporosis-pseudoglioma syndrome Other syndrome with[se-atlas.de]

  • Autosomal Dominant Hyper-IgE Syndrome

    Peripheral and brain artery abnormalities Coronary artery abnormalities : ectasias and aneurysm In mouse model, inhibited STAT3 signaling and IL-17A blockage resulted in increased[slideshare.net] Patients have coarse facial features, delayed shedding of baby teeth, osteopenia, and recurrent fractures.[msdmanuals.com] Osteopenia or osteoporosis was found in 79% of children and adults.[ncbi.nlm.nih.gov]

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