Showing 1 - 10 results of 10 for search 'A. Ndatinya', query time: 0.03s Refine Results
  1. 1
    Turner syndrome in childhood period – A case Report

    Turner syndrome in childhood period – A case Report by B. Tuyishimire, O. Karangwa, F. Rutagarama, A. Ndatinya, C. Nsanzabaganwa, L. Mutesa

    Published 2022-06-01
    Article
  2. 2
    Turner syndrome in childhood period – A case Report

    Turner syndrome in childhood period – A case Report by B. Tuyishimire, O. Karangwa, F. Rutagarama, A. Ndatinya, C. Nsanzabaganwa, L. Mutesa

    Published 2022-06-01
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    Article
  3. 3
    Diagnosis of Treacher-Collins Syndrome: The role of the multidisciplinary team in patient management and family genetic counseling

    Diagnosis of Treacher-Collins Syndrome: The role of the multidisciplinary team in patient management and family genetic counseling by B. Tuyishimire, H. Irere, C. Muhizi, A. Ndatinya, O. R. Karangwa, F. Rutarama, C. Nsanzabaganwa, L. Mutesa

    Published 2022-12-01
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  4. 4
    Management challenges of disorders of sex development- Case Series

    Management challenges of disorders of sex development- Case Series by B. Tuyishimire, H. Irere, F. Rutagarama, A. Ndatinya, O.R. Karangwa, A. Gasana, C. Nsanzabaganwa, L. Mutesa

    Published 2022-09-01
    Article
  5. 5
    Management challenges of disorders of sex development- Case Series

    Management challenges of disorders of sex development- Case Series by B. Tuyishimire, H. Irere, F. Rutagarama, A. Ndatinya, O. R. Karangwa, A. Gasana, C. Nsanzabaganwa, L. Mutesa

    Published 2022-09-01
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    Article
  6. 6
    Neurofibromatosis type 1 – A clinical case report and management review

    Neurofibromatosis type 1 – A clinical case report and management review by C. Muhizi, H. Irere, B. Tuyishimire, A. Ndatinya, O. R. Karangwa, F. Rutagarama, C. Nsanzabaganwa, L. Mutesa

    Published 2022-12-01
    Article
  7. 7
    INTRODUCTION: Neurofibromatosis Type 1 (NF1) or Von Recklinghausen’s disease, is a rare genetic disease characterized by multiple benign tumors of nerves and skin (neurofibromas), and skin decorations. However, it is multisystem and can affect each organ in the body, leading to debilitating effects. CLINICAL CASE: We present a case of an 18-year-old girl with NF1. The disease onset started in childhood at the age of 3 years with the appearance of hyperpigmented skin macules. Her mother also presented with multiple nodules on the face and trunk, and her little brother was reported to have disseminated macules. She had poor performance at school and delayed menses. The diagnosis of NF-1 was made, and a multidisciplinary team was involved in management of the patient CONCLUSION: Although genetic testing and confirmation are available, NF1 remains a clinical diagnosis and requires management by multidisciplinary team

    INTRODUCTION: Neurofibromatosis Type 1 (NF1) or Von Recklinghausen’s disease, is a rare genetic disease characterized by multiple benign tumors of nerves and skin (neurofibromas),... by B. Tuyishimire, H. Irere, C. Muhizi, A. Ndatinya, O. R. Karangwa, F. Rutagarama, C. Nsanzabaganwa, L. Mutesa

    Published 2022-12-01
    Article
  8. 8
    Neurofibromatosis type 1 – A clinical case report and management review

    Neurofibromatosis type 1 – A clinical case report and management review by C. Muhizi, H. Irere, B. Tuyishimire, A. Ndatinya, O. R. Karangwa, F. Rutarama, L. Mutesa, C. Nsanzabaganwa, L. Mutesa

    Published 2022-12-01
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    Article
  9. 9
    The diagnosis of Beckwith-Wiedemann syndrome in a child and psychological implications to parents – A case report

    The diagnosis of Beckwith-Wiedemann syndrome in a child and psychological implications to parents – A case report by B. Tuyishimire, H. Irere, N. Dukuze, B. Iradukunda, C. Muhizi, A. Ndatinya, O. R. Karangwa, F. Rutagarama, C. Nsanzabaganwa, L. Mutesa

    Published 2023-03-01
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  10. 10
    Genetic and phenotypic presentation of Usher syndrome - a case report

    Genetic and phenotypic presentation of Usher syndrome - a case report by N. Dukuze, E. Uwibambe, P. Sesonga, J. Niyongere, B. Tuyishimire, A. Urungwiro, J. Ndinkabandi, A. Rwamatwara, S. Niyoyita, G. Isingizwe, J. Mutamuliza, C. Nsanzabaganwa, J. Bukuru, F. Rutagarama, O. Karangwa, A. Ndatinya, C. Muhizi, L. Mutesa

    Published 2024-01-01
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