The Experts below are selected from a list of 207 Experts worldwide ranked by ideXlab platform

Murat Derbent - One of the best experts on this subject based on the ideXlab platform.

  • PHACES Syndrome with small, late-onset hemangiomas
    European Journal of Pediatrics, 2007
    Co-Authors: Bırgın Torer, Hande Gulcan, Hasan Kilicdag, Murat Derbent
    Abstract:

    Although hemangiomas are the hallmark of the PHACES Syndrome, they may be nonexistent at birth and may not develop until later in early infancy. We report an infant who presented initially with cardiac defect, sternal nonunion, supraumbilical raphé, and congenital hypothyroidism without any hemangioma, and who subsequently developed facial hemangiomas at 2 months of age. We noted that there is a possibility that hemangiomas may subsequently develop later in early infancy and congenital hypothyroidism may be associated with the PHACES Syndrome.

  • PHACES Syndrome with small late onset hemangiomas
    European Journal of Pediatrics, 2007
    Co-Authors: Bırgın Torer, Hande Gulcan, Hasan Kilicdag, Murat Derbent
    Abstract:

    Although hemangiomas are the hallmark of the PHACES Syndrome, they may be nonexistent at birth and may not develop until later in early infancy. We report an infant who presented initially with cardiac defect, sternal nonunion, supraumbilical raphe, and congenital hypothyroidism without any hemangioma, and who subsequently developed facial hemangiomas at 2 months of age. We noted that there is a possibility that hemangiomas may subsequently develop later in early infancy and congenital hypothyroidism may be associated with the PHACES Syndrome.

Bırgın Torer - One of the best experts on this subject based on the ideXlab platform.

  • PHACES Syndrome with small, late-onset hemangiomas
    European Journal of Pediatrics, 2007
    Co-Authors: Bırgın Torer, Hande Gulcan, Hasan Kilicdag, Murat Derbent
    Abstract:

    Although hemangiomas are the hallmark of the PHACES Syndrome, they may be nonexistent at birth and may not develop until later in early infancy. We report an infant who presented initially with cardiac defect, sternal nonunion, supraumbilical raphé, and congenital hypothyroidism without any hemangioma, and who subsequently developed facial hemangiomas at 2 months of age. We noted that there is a possibility that hemangiomas may subsequently develop later in early infancy and congenital hypothyroidism may be associated with the PHACES Syndrome.

  • PHACES Syndrome with small late onset hemangiomas
    European Journal of Pediatrics, 2007
    Co-Authors: Bırgın Torer, Hande Gulcan, Hasan Kilicdag, Murat Derbent
    Abstract:

    Although hemangiomas are the hallmark of the PHACES Syndrome, they may be nonexistent at birth and may not develop until later in early infancy. We report an infant who presented initially with cardiac defect, sternal nonunion, supraumbilical raphe, and congenital hypothyroidism without any hemangioma, and who subsequently developed facial hemangiomas at 2 months of age. We noted that there is a possibility that hemangiomas may subsequently develop later in early infancy and congenital hypothyroidism may be associated with the PHACES Syndrome.

Hasan Kilicdag - One of the best experts on this subject based on the ideXlab platform.

  • PHACES Syndrome with small, late-onset hemangiomas
    European Journal of Pediatrics, 2007
    Co-Authors: Bırgın Torer, Hande Gulcan, Hasan Kilicdag, Murat Derbent
    Abstract:

    Although hemangiomas are the hallmark of the PHACES Syndrome, they may be nonexistent at birth and may not develop until later in early infancy. We report an infant who presented initially with cardiac defect, sternal nonunion, supraumbilical raphé, and congenital hypothyroidism without any hemangioma, and who subsequently developed facial hemangiomas at 2 months of age. We noted that there is a possibility that hemangiomas may subsequently develop later in early infancy and congenital hypothyroidism may be associated with the PHACES Syndrome.

  • PHACES Syndrome with small late onset hemangiomas
    European Journal of Pediatrics, 2007
    Co-Authors: Bırgın Torer, Hande Gulcan, Hasan Kilicdag, Murat Derbent
    Abstract:

    Although hemangiomas are the hallmark of the PHACES Syndrome, they may be nonexistent at birth and may not develop until later in early infancy. We report an infant who presented initially with cardiac defect, sternal nonunion, supraumbilical raphe, and congenital hypothyroidism without any hemangioma, and who subsequently developed facial hemangiomas at 2 months of age. We noted that there is a possibility that hemangiomas may subsequently develop later in early infancy and congenital hypothyroidism may be associated with the PHACES Syndrome.

Hande Gulcan - One of the best experts on this subject based on the ideXlab platform.

  • PHACES Syndrome with small, late-onset hemangiomas
    European Journal of Pediatrics, 2007
    Co-Authors: Bırgın Torer, Hande Gulcan, Hasan Kilicdag, Murat Derbent
    Abstract:

    Although hemangiomas are the hallmark of the PHACES Syndrome, they may be nonexistent at birth and may not develop until later in early infancy. We report an infant who presented initially with cardiac defect, sternal nonunion, supraumbilical raphé, and congenital hypothyroidism without any hemangioma, and who subsequently developed facial hemangiomas at 2 months of age. We noted that there is a possibility that hemangiomas may subsequently develop later in early infancy and congenital hypothyroidism may be associated with the PHACES Syndrome.

  • PHACES Syndrome with small late onset hemangiomas
    European Journal of Pediatrics, 2007
    Co-Authors: Bırgın Torer, Hande Gulcan, Hasan Kilicdag, Murat Derbent
    Abstract:

    Although hemangiomas are the hallmark of the PHACES Syndrome, they may be nonexistent at birth and may not develop until later in early infancy. We report an infant who presented initially with cardiac defect, sternal nonunion, supraumbilical raphe, and congenital hypothyroidism without any hemangioma, and who subsequently developed facial hemangiomas at 2 months of age. We noted that there is a possibility that hemangiomas may subsequently develop later in early infancy and congenital hypothyroidism may be associated with the PHACES Syndrome.

P. Tortori-donati - One of the best experts on this subject based on the ideXlab platform.

  • Posterior fossa and arterial abnormalities in patients with facial capillary haemangioma: presumed incomplete phenotypic expression of PHACES Syndrome
    Neuroradiology, 2001
    Co-Authors: A. Rossi, G. L. Bava, R. Biancheri, P. Tortori-donati
    Abstract:

    We report on the neuroradiological studies performed on three infants with capillary haemangioma (CH) of the head and neck with associated posterior fossa and arterial abnormalities. Posterior fossa malformations were represented by cerebellar hemispheric and vermian hypoplasia and cerebellar cortical dysgenesis, whereas arterial anomalies included bilateral agenesis, kinking, and looping of the internal carotid arteries. One patient had marked exophthalmos due to intraorbital CH. We suggest that these patients had an incomplete phenotypic expression of PHACES Syndrome, a vascular phakomatosis characterised by the variable association of posterior fossa malformations, CH, arterial anomalies, coarctation of the aorta and cardiac defects, eye abnormalities, and sternal and medioventral defects. Evidence suggests that PHACES Syndrome is not a random association but a true phakomatosis; further studies are awaited to shed light on a possible genetic background. The phenotypic spectrum is broad and still largely unexplored, and precise diagnostic criteria have not yet been identified. A causal teratogenic influence, possibly related to anomalous expression of vascular growth factors and their modulators, is suggested to occur between gestational weeks 3 and 5.5