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Carlo Bellini - One of the best experts on this subject based on the ideXlab platform.

  • Aplasia cutis congenita, Skull Defect, brain heterotopia, and intestinal lymphangiectasia.
    American journal of medical genetics. Part A, 2005
    Co-Authors: Eugenio Bonioli, Gianantonio Spena, Guido Morcaldi, Antonio Di Stefano, Giovanni Serra, Raoul C M Hennekam, Carlo Bellini
    Abstract:

    We describe a female infant with a previously unreported combination of manifestations characterized by aplasia cutis, Skull Defect, brain heterotopia, mild congenital lymphedema, and intestinal lymphangiectasia. The association of intestinal lymphangiectasia and aplasia cutis, and the association of intestinal lymphangiectasia with brain heterotopia in the lymphedema-lymphangiectasia-mental retardation syndrome have been described in single reports. In one family, the association of cortical dysplasia and congenital lymphedema have been related to mutations in the RELN gene.

  • Aplasia cutis congenita, Skull Defect, brain heterotopia, and intestinal lymphangiectasia.
    American Journal of Medical Genetics Part A, 2005
    Co-Authors: Eugenio Bonioli, Gianantonio Spena, Guido Morcaldi, Antonio Di Stefano, Giovanni Serra, Raoul C M Hennekam, Carlo Bellini
    Abstract:

    We describe a female infant with a previously unreported combination of manifestations characterized by aplasia cutis, Skull Defect, brain heterotopia, mild congenital lymphedema, and intestinal lymphangiectasia. The association of intestinal lymphangiectasia and aplasia cutis, and the association of intestinal lymphangiectasia with brain heterotopia in the lymphedema-lymphangiectasia-mental retardation syndrome have been described in single reports. In one family, the association of cortical dysplasia and congenital lymphedema have been related to mutations in the RELN gene. (C) 2004 Wiley-Liss, Inc.

  • Aplasia cutis congenita, Skull Defect, brain heterotopia, and intestinal lymphangiectasia.
    American journal of medical genetics. Part A, 2005
    Co-Authors: Eugenio Bonioli, Gianantonio Spena, Guido Morcaldi, Antonio Di Stefano, Giovanni Serra, Raoul C M Hennekam, Carlo Bellini
    Abstract:

    We describe a female infant with a previously unreported combination of manifestations characterized by aplasia cutis, Skull Defect, brain heterotopia, mild congenital lymphedema, and intestinal lymphangiectasia. The association of intestinal lymphangiectasia and aplasia cutis, and the association of intestinal lymphangiectasia with brain heterotopia in the lymphedema-lymphangiectasia-mental retardation syndrome have been described in single reports. In one family, the association of cortical dysplasia and congenital lymphedema have been related to mutations in the RELN gene.

Zeng Wensheng - One of the best experts on this subject based on the ideXlab platform.

  • repair of Skull Defect treated with self Skull external lamina
    Journal of Gannan Medical University, 2007
    Co-Authors: Zeng Wensheng
    Abstract:

    Objective:To discuss the clinic applications to the repair of Skull Defect with self Skull external lamina.Methods:The Skull Defect is repaired by using the home-made tools to acquire Skull external lamina ,according to the size of the Defect.Results:It is safe and secure to acquire the Skull external lamina by using the home-made tools.20 patients with different sizes of Skull Defect were successfully treated with self external lamina,with satisfied outlook and good fixation and no complications.Its tissue compatibility,stability,security is good.Conclusion:The method of repairing Skull Defect by self Skull external lamina is with good effect and worth promoting.

Eugenio Bonioli - One of the best experts on this subject based on the ideXlab platform.

  • Aplasia cutis congenita, Skull Defect, brain heterotopia, and intestinal lymphangiectasia.
    American journal of medical genetics. Part A, 2005
    Co-Authors: Eugenio Bonioli, Gianantonio Spena, Guido Morcaldi, Antonio Di Stefano, Giovanni Serra, Raoul C M Hennekam, Carlo Bellini
    Abstract:

    We describe a female infant with a previously unreported combination of manifestations characterized by aplasia cutis, Skull Defect, brain heterotopia, mild congenital lymphedema, and intestinal lymphangiectasia. The association of intestinal lymphangiectasia and aplasia cutis, and the association of intestinal lymphangiectasia with brain heterotopia in the lymphedema-lymphangiectasia-mental retardation syndrome have been described in single reports. In one family, the association of cortical dysplasia and congenital lymphedema have been related to mutations in the RELN gene.

  • Aplasia cutis congenita, Skull Defect, brain heterotopia, and intestinal lymphangiectasia.
    American Journal of Medical Genetics Part A, 2005
    Co-Authors: Eugenio Bonioli, Gianantonio Spena, Guido Morcaldi, Antonio Di Stefano, Giovanni Serra, Raoul C M Hennekam, Carlo Bellini
    Abstract:

    We describe a female infant with a previously unreported combination of manifestations characterized by aplasia cutis, Skull Defect, brain heterotopia, mild congenital lymphedema, and intestinal lymphangiectasia. The association of intestinal lymphangiectasia and aplasia cutis, and the association of intestinal lymphangiectasia with brain heterotopia in the lymphedema-lymphangiectasia-mental retardation syndrome have been described in single reports. In one family, the association of cortical dysplasia and congenital lymphedema have been related to mutations in the RELN gene. (C) 2004 Wiley-Liss, Inc.

  • Aplasia cutis congenita, Skull Defect, brain heterotopia, and intestinal lymphangiectasia.
    American journal of medical genetics. Part A, 2005
    Co-Authors: Eugenio Bonioli, Gianantonio Spena, Guido Morcaldi, Antonio Di Stefano, Giovanni Serra, Raoul C M Hennekam, Carlo Bellini
    Abstract:

    We describe a female infant with a previously unreported combination of manifestations characterized by aplasia cutis, Skull Defect, brain heterotopia, mild congenital lymphedema, and intestinal lymphangiectasia. The association of intestinal lymphangiectasia and aplasia cutis, and the association of intestinal lymphangiectasia with brain heterotopia in the lymphedema-lymphangiectasia-mental retardation syndrome have been described in single reports. In one family, the association of cortical dysplasia and congenital lymphedema have been related to mutations in the RELN gene.

Raoul C M Hennekam - One of the best experts on this subject based on the ideXlab platform.

  • Aplasia cutis congenita, Skull Defect, brain heterotopia, and intestinal lymphangiectasia.
    American journal of medical genetics. Part A, 2005
    Co-Authors: Eugenio Bonioli, Gianantonio Spena, Guido Morcaldi, Antonio Di Stefano, Giovanni Serra, Raoul C M Hennekam, Carlo Bellini
    Abstract:

    We describe a female infant with a previously unreported combination of manifestations characterized by aplasia cutis, Skull Defect, brain heterotopia, mild congenital lymphedema, and intestinal lymphangiectasia. The association of intestinal lymphangiectasia and aplasia cutis, and the association of intestinal lymphangiectasia with brain heterotopia in the lymphedema-lymphangiectasia-mental retardation syndrome have been described in single reports. In one family, the association of cortical dysplasia and congenital lymphedema have been related to mutations in the RELN gene.

  • Aplasia cutis congenita, Skull Defect, brain heterotopia, and intestinal lymphangiectasia.
    American Journal of Medical Genetics Part A, 2005
    Co-Authors: Eugenio Bonioli, Gianantonio Spena, Guido Morcaldi, Antonio Di Stefano, Giovanni Serra, Raoul C M Hennekam, Carlo Bellini
    Abstract:

    We describe a female infant with a previously unreported combination of manifestations characterized by aplasia cutis, Skull Defect, brain heterotopia, mild congenital lymphedema, and intestinal lymphangiectasia. The association of intestinal lymphangiectasia and aplasia cutis, and the association of intestinal lymphangiectasia with brain heterotopia in the lymphedema-lymphangiectasia-mental retardation syndrome have been described in single reports. In one family, the association of cortical dysplasia and congenital lymphedema have been related to mutations in the RELN gene. (C) 2004 Wiley-Liss, Inc.

  • Aplasia cutis congenita, Skull Defect, brain heterotopia, and intestinal lymphangiectasia.
    American journal of medical genetics. Part A, 2005
    Co-Authors: Eugenio Bonioli, Gianantonio Spena, Guido Morcaldi, Antonio Di Stefano, Giovanni Serra, Raoul C M Hennekam, Carlo Bellini
    Abstract:

    We describe a female infant with a previously unreported combination of manifestations characterized by aplasia cutis, Skull Defect, brain heterotopia, mild congenital lymphedema, and intestinal lymphangiectasia. The association of intestinal lymphangiectasia and aplasia cutis, and the association of intestinal lymphangiectasia with brain heterotopia in the lymphedema-lymphangiectasia-mental retardation syndrome have been described in single reports. In one family, the association of cortical dysplasia and congenital lymphedema have been related to mutations in the RELN gene.

Gianantonio Spena - One of the best experts on this subject based on the ideXlab platform.

  • Aplasia cutis congenita, Skull Defect, brain heterotopia, and intestinal lymphangiectasia.
    American journal of medical genetics. Part A, 2005
    Co-Authors: Eugenio Bonioli, Gianantonio Spena, Guido Morcaldi, Antonio Di Stefano, Giovanni Serra, Raoul C M Hennekam, Carlo Bellini
    Abstract:

    We describe a female infant with a previously unreported combination of manifestations characterized by aplasia cutis, Skull Defect, brain heterotopia, mild congenital lymphedema, and intestinal lymphangiectasia. The association of intestinal lymphangiectasia and aplasia cutis, and the association of intestinal lymphangiectasia with brain heterotopia in the lymphedema-lymphangiectasia-mental retardation syndrome have been described in single reports. In one family, the association of cortical dysplasia and congenital lymphedema have been related to mutations in the RELN gene.

  • Aplasia cutis congenita, Skull Defect, brain heterotopia, and intestinal lymphangiectasia.
    American Journal of Medical Genetics Part A, 2005
    Co-Authors: Eugenio Bonioli, Gianantonio Spena, Guido Morcaldi, Antonio Di Stefano, Giovanni Serra, Raoul C M Hennekam, Carlo Bellini
    Abstract:

    We describe a female infant with a previously unreported combination of manifestations characterized by aplasia cutis, Skull Defect, brain heterotopia, mild congenital lymphedema, and intestinal lymphangiectasia. The association of intestinal lymphangiectasia and aplasia cutis, and the association of intestinal lymphangiectasia with brain heterotopia in the lymphedema-lymphangiectasia-mental retardation syndrome have been described in single reports. In one family, the association of cortical dysplasia and congenital lymphedema have been related to mutations in the RELN gene. (C) 2004 Wiley-Liss, Inc.

  • Aplasia cutis congenita, Skull Defect, brain heterotopia, and intestinal lymphangiectasia.
    American journal of medical genetics. Part A, 2005
    Co-Authors: Eugenio Bonioli, Gianantonio Spena, Guido Morcaldi, Antonio Di Stefano, Giovanni Serra, Raoul C M Hennekam, Carlo Bellini
    Abstract:

    We describe a female infant with a previously unreported combination of manifestations characterized by aplasia cutis, Skull Defect, brain heterotopia, mild congenital lymphedema, and intestinal lymphangiectasia. The association of intestinal lymphangiectasia and aplasia cutis, and the association of intestinal lymphangiectasia with brain heterotopia in the lymphedema-lymphangiectasia-mental retardation syndrome have been described in single reports. In one family, the association of cortical dysplasia and congenital lymphedema have been related to mutations in the RELN gene.