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1,605 Possible Causes for 10, CONE ROD, DYSTROPHY

Did you mean: 10, CONE, ROD, DYSTROPHY

  • Osteoporosis

    Abstract Duchenne muscular dystrophy (DMD) is an X-linked recessive muscle disease characterized by secondary osteoporosis and increased fractures.[ncbi.nlm.nih.gov] KEYWORDS: Chronic kidney disease; biomarkers; bone mineral density; dialysis; fractures; histomorphometry; imaging; osteoporosis; renal osteodystrophy[ncbi.nlm.nih.gov] Vertebral fractures were diagnosed on CT preformed 10 years after the original CT and through online medical records.[ncbi.nlm.nih.gov]

  • Retinal Dystrophy

    KEYWORDS: CRB1; retinal capillaritis; retinal dystrophy; retinitis pigmentosa; uveitis[ncbi.nlm.nih.gov] Re: Cone Rod Retinal Dystrophy Posted by kamshar20 on 5/12/2016 at 10:21 AM My son 9 years old has been diagnosed rod cone dystrophy when he was 5 years old.[afb.org] H35.52 to ICD-9-CM Code History 2016 (effective 10/1/2015) : New code (first year of non-draft ICD-10-CM) 2017 (effective 10/1/2016) : No change 2018 (effective 10/1/2017)[icd10data.com]

  • Limb-Girdle Muscular Dystrophy

    Abstract Emery-Dreifuss muscular dystrophy (EDMD) and limb-girdle muscular dystrophy type 1B (LGMD1B) are characterized by cardiac dysrhythmias, late-onset cardiomyopathy,[ncbi.nlm.nih.gov] Here, we characterized a family with early onset cone-rod dystrophy (CRD) and muscular dystrophy.[ncbi.nlm.nih.gov] Code History 2016 (effective 10/1/2015) : New code (first year of non-draft ICD-10-CM) 2017 (effective 10/1/2016) : No change 2018 (effective 10/1/2017) : No change 2019 ([icd10data.com]

  • Williams Syndrome

    PURPOSE: To describe a case of rod-cone dystrophy associated with Williams syndrome. METHODS: This is an observational case report. The medical history was assessed.[ncbi.nlm.nih.gov] Autism Res 2017, 10: 99-112. 2016 International Society for Autism Research, Wiley Periodicals, Inc.[ncbi.nlm.nih.gov] Review of the echocardiographic database of our institution over a 10-year period identified 26 other patients with Williams syndrome.[ncbi.nlm.nih.gov]

  • Liver Cirrhosis

    OBJECTIVE: Though the liver is frequently affected in myotonic dystrophy type 1 and 2 (DM1, DM2), non-alcoholic and non-hepatitic liver cirrhosis have not been reported as[ncbi.nlm.nih.gov] Abstract Alström syndrome is a rare autosomal recessive genetic disorder characterized by cone-rod dystrophy, hearing loss, childhood truncal obesity, insulin resistance and[ncbi.nlm.nih.gov] For such conditions the ICD-10-CM has a coding convention that requires the underlying condition be sequenced first followed by the manifestation.[icd10data.com]

  • CINCA Syndrome

    A state of severe retinal dystrophy of post-inflammatory origin became evident on funduscopy, optical coherence tomography and visual electrophysiology tests at the age of[ncbi.nlm.nih.gov] We report the cases of monozygotic twins with CINCA syndrome whose predominant ocular manifestation was inflammatory rod-cone retinal dystrophy.[ncbi.nlm.nih.gov] This is the American ICD-10-CM version of M04.2 - other international versions of ICD-10 M04.2 may differ.[icd10data.com]

  • Progressive Cone Dystrophy

    Abstract Psychophysical, reflectometric, and electrophysiological studies were performed on four members of a dominant pedigree with progressive cone dystrophy.[ncbi.nlm.nih.gov] Cone-rod dystrophy results from a primary loss of cone photoreceptors, followed by loss of rods.[blindness.org] Cone system psychophysical thresholds were elevated for targets presented within the central 10 degrees, but were within normal limits for targets at peripheral locations.[ncbi.nlm.nih.gov]

  • Deferoxamine

    KEYWORDS: Deferoxamine; Drug toxicity; Pattern dystrophy; Thalassemia[ncbi.nlm.nih.gov] Patients (17 of 60; 28.3%) achieved mT2* 10 ms and 10% increase from baseline at month 24; 15 switched to monotherapy during the study based on favorable mT2*.[ncbi.nlm.nih.gov] DEFENSES AND INFECTIOUS COMPLICATIONS IN MAINTENANCE HEMODIALYSIS PATIENTS 865 DIALYSIS ASSOCIATED HEPATITIS 881 DIALYSIS IN THE ACQUIRED IMMUNODEFICIENCY SYNDROME 904 44 RENAL[books.google.com]

  • Retinal Detachment

    Abstract Two eyes of 2 patients with macular hole-associated retinal detachment in clinically diagnosed vitelliruptive stage of Best vitelliform dystrophy were surgically[ncbi.nlm.nih.gov] The outer layer - the retinal pigment epithelium (RPE) - is a layer of cells behind the rods and cones. The RPE helps to nourish and support the rods and cones.[patient.info] 1/2015) : New code (first year of non-draft ICD-10-CM) 2017 (effective 10/1/2016) : No change 2018 (effective 10/1/2017) : No change 2019 (effective 10/1/2018) : No change[icd10data.com]

  • Amblyopia

    We studied four consecutive children with posterior polymorphous dystrophy who had coexisting astigmatism.[ncbi.nlm.nih.gov] The full-field electroretinography was normal in the right eye, but rod response, cone response, and combined response were non-recordable, and 30-Hz response was very small[ncbi.nlm.nih.gov] Results: Our study revealed that suppression changes across the central 10 visual field by mean luminance modulation in amblyopes as well as normal controls.[ncbi.nlm.nih.gov]