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142 Possible Causes for Coronary Artery Disease, Retinal Pigmentation, Round Face

  • Mucopolysaccharidosis

    pigment epithelium.[ncbi.nlm.nih.gov] 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] Defining this natural history is essential for a proper comparison with Hunter patients receiving systemic treatment, thus determining if it can or cannot improve retinal[ncbi.nlm.nih.gov]

  • Mucopolysaccharidosis 2

    Abnormal retinal pigmentation and papilloedema - leading to visual impairment. Type B - mild form This usually presents later and may not be noticed until adulthood.[patient.info] A thickened myocardium eventually leads to coronary artery compromise, myocardial disease, and, in conjunction with airway disease, pulmonary hypertension.[emedicine.medscape.com]

  • Mucopolysaccharidosis 1

    Figure 4 Retinal pigment epithelial changes in a 15-year-old patient with MPS IH/S Hurler/Scheie. A total of 13 patients with MPS IH Hurler had undergone ERGs.[nature.com] Caution should be exercised if epinephrine is being considered for use in patients with MPS I due to the increased prevalence of coronary artery disease in these patients.[aldurazyme.com] Retinal pigment epithelial atrophic changes were documented in two (11%) patients with MPS IH Hurler, five (56%) patients with MPS IH/S Hurler/Scheie ( Figure 4 ), and two[nature.com]

  • Pseudoxanthoma Elasticum

    Current clinical measures of retinal pigment epithelial health only look for areas of cell death, as in geographic atrophy.[ncbi.nlm.nih.gov] Our patient was previously treated for retinal and gastrointestinal hemorrhage and coronary artery disease, and is under surveillance for cerebral aneurysms.[ncbi.nlm.nih.gov] Face Tổng hợp Faces FIFA 16. Join the discussion or compare with others! Parigini, Vittorio: 18: Torino: 7.[ecyquzuralin.tk]

  • Macular Degeneration

    She presented with visual distortion in her right eye and was found to have a retinal pigment epithelial detachment (RPED) on optical coherence tomography (OCT).[ncbi.nlm.nih.gov] Compared to patients with PCV, patients with nAMD were more likely to be older and suffer from hyperlipidemia, coronary artery disease, rheumatism, and tumor.[ncbi.nlm.nih.gov] Polyps appears as round multiple heterogeneous hyperreflective structures. Figure 29. SS-OCT and en-face OCT of a patients with late AMD with geography atrophy.[amdbook.org]

  • Amyloidosis

    The circulating protein is synthesized predominantly in the liver, but there is also important local production in the eye by retinal pigment epithelial cells and by the choroid[nejm.org] Weight gain and rounded face. Muscle weakness (uncommon when used intermittently as for treating amyloidosis). Vaginal yeast infection.[circ.ahajournals.org] Transthyretin (TTR) is a homotetramer plasma transport protein secreted primarily by liver but also in retinal pigment epithelium and choroid plexus.[intechopen.com]

  • Best Disease

    retinal pigment epithelium and photoreceptors.[ncbi.nlm.nih.gov] […] in patients with more severe disease and with impaired left ventricular function. 1 Furthermore, coronary artery bypass grafting is remarkably safe.[bmj.com] The macula is responsible for sharp central vision, which is needed for detailed tasks such as reading, driving, and recognizing faces.[en.wikipedia.org]

  • Cockayne Syndrome

    The twins were deaf and blind, with optic atrophy and retinal pigmentation, while their brother had cataracts.[onlinelibrary.wiley.com] Congenital neurobehavioral disorder characterized by rounded face, low forehead, almond shaped eyes, squinting, hypogonadism, hypotonia, insatiable appetite leading to obesity[icd10data.com] pigment, miotic pupils may be difficult to dilate, cataracts, optic atrophy Teeth Dental caries Bloom syndrome (p. 234) Roth m u nd Thomson syndrome (p. 238) Hartnup syndrome[cram.com]

  • Kearns Sayre Syndrome

    The triad of progressive external ophthalmoplegia, atypical retinal pigmentation and cardiac conduction defects characterizes Kearns-Sayre syndrome (KSS), which is most often[ncbi.nlm.nih.gov] A randomized study of the prevention of sudden death in patients with coronary artery disease. N Engl J Med. 1999; 341 : 1882–1890.[doi.org] Her face was an unexpressed-rounded and greasy one with an incomplete palpebral ptosis bilaterally (Figure 1), the nails and teeth were normal She was very thin owing to generalized[ispub.com]

  • Choroiditis

    Multifocal choroiditis is an inflammatory disorder affecting the outer photoreceptors, ellipsoid layer, retinal pigment epithelium, and choroid; and areas of acute inflammation[ncbi.nlm.nih.gov] Medical History: Coronary artery disease. History of MI with stent placement. Current Meds : Prednisone, 5 mg PO daily.[webeye.ophth.uiowa.edu] The pupils were equally round and reactive with no relative afferent papillary defect.[retinalphysician.com]

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