Publications by authors named "Seref Etker"

Background: In the normal human penis, the glans wings merge in the midline ventrally, but are separated by the 'septum glandis' in conjunction with the frenulum. The frenulum is also included in the formation of the distal (glanular and subcoronal) urethra, which has a special part known as the 'fossa navicularis'. This has inspired a hypospadias repair technique that simulates the development of the glanular and subcoronal urethra, which can be incorporated into the repair of all cases of hypospadias.

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Amália Frisch was born in Edirne/Adrianople, Turkey, in 1882 to an immigrant Jewish family from Hungary. Following her graduation from the American College for Girls in Istanbul in 1901, she traveled to Switzerland for her medical education. Amália Frisch graduated from the school of medicine in Bern in 1907, and received her MD (Doctor universae medicinae) degree from the Zurich University in 1908.

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Background: Disorders of sexual development (DSD) are congenital conditions in which the development of the chromosomal, gonadal or anatomical sex can be deemed atypical. The external genitalia should appear 'normal' in size and shape from birth, with no question of abnormality, and the individual must receive appropriate social-environmental feedback in the course of the sexual maturation process.

Methods: We review regional differences in the variables considered important for gender assignment in individuals with DSD.

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Although primary bronchopulmonary fibrosarcoma is a rare tumor, it may be characterized by the symptoms of acute respiratory distress occurring during the first moments of life in a newborn. It is one of the leading congenital malignant neoplasms of the lung, but is considered a borderline tumor since its biological behavior is much more favorable than that of adult fibrosarcomas. In the absence of metastases, complete resection is curative.

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Objective: Cloacal dysgenesis sequence is a lethal malformation, which usually requires termination. In this study, our aim was to evaluate the prenatal and postnatal diagnostic features of cloacal dysgenesis sequence and review the management of the patients.

Material And Methods: The data of six cases of cloacal dysgenesis sequences were collected from the ultrasonography and neonatal records.

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