Yazar "Yuca, Sevil Ari" seçeneğine göre listele

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    The 46XX Ovotesticular Disorders of Sexual Development with Dismorphic Features
    (Elsevier Science Inc, 2015) Eklioglu, Beray Selver; Atabek, Mehmet Emre; Akyurek, Nesibe; Yuca, Sevil Ari; Piskin, Mesut
    Background: Ovotesticular disorders of sexual development (OT-DSD) represent a rare sex development disorder characterized by the presence of both ovarian and testicular tissues in the same or the contralateral gonad. Case: We present the case of a 14-year-old female patient with signs of virilization at a pubertal age and with dysmorphic features, diagnosed as 46, XX OT-DSD. Conclusion: We want to point out that patients with 46 XX OT-DSD may present with virilization at puberty and may be accompanied by dysmorphic features.
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    The effects of omega-3 fatty acids on exercise induced bronchospasm in nonasthmatic obese and non-obese children
    (Wiley-Blackwell, 2015) Ozdemir, Ayse; Okudan, Nilsel; Yuca, Sevil Ari; Belviranli, Muaz; Gokbel, Hakki
    [Abstract Not Availabe]
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    Partial Merosin Deficiency and Precocious Puberty
    (Modestum Ltd, 2015) Eklioglu, Beray Selver; Akyurek, Nesibe; Yuca, Sevil Ari; Atabek, Mehmet Emre
    The congenital muscular dystrophies (CMD) are autosomal-recessive disorders. Classical congenital muscular dystrophy is grouped as merosin-positive and merosin-negative (MN-CMD). Precocious puberty in girls has been defined by Marshal and Tanner in 1969. In most of the cases, precocious puberty is idiopathic and is related to premature release of gonadotrophins. So far, the association between merosin deficiency and precocious puberty has not been identified. We report a case of a child with precocious puberty who was diagnosed with merosin deficiency in infancy.
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    Partial Merosin Deficiency and Precocious Puberty
    (Modestum Ltd, 2015) Eklioglu, Beray Selver; Akyurek, Nesibe; Yuca, Sevil Ari; Atabek, Mehmet Emre
    The congenital muscular dystrophies (CMD) are autosomal-recessive disorders. Classical congenital muscular dystrophy is grouped as merosin-positive and merosin-negative (MN-CMD). Precocious puberty in girls has been defined by Marshal and Tanner in 1969. In most of the cases, precocious puberty is idiopathic and is related to premature release of gonadotrophins. So far, the association between merosin deficiency and precocious puberty has not been identified. We report a case of a child with precocious puberty who was diagnosed with merosin deficiency in infancy.
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    Type 1 Diabetes Mellitus Associated with Autoimmune Thyroid Disease, Celiac Disease and Facial Asymmetry
    (Modestum Ltd, 2014) Akyurek, Nesibe; Atabek, Mehmet Emre; Eklioglu, Beray Selver; Yuca, Sevil Ari
    Patients with type 1 diabetes mellitus are at a great risk of developing other autoimmune diseases. Ten -year-old girl was brought to our clinic with complaints of polydipsia, polyuria and weight loss and was diagnosed as diabetic ketoacidosis due to autoimmune type 1 DM. On physical examination, on the left side of her face mild facial asymmetry was noticed. She had the asymmetry since the birth. Elevated thyroid antibodies associated with diffuse goiter and hypothyroidism led to the diagnosis of autoimmune thyroid disease, and elevated antiendomysial antibodies, anti-gliadin antibodies and abnormal intestinal biopsy findings led to the diagnosis of celiac disease. To our knowledge, this is the first report on a child with a combination type 1 diabetes mellitus, autoimmune thyroid disease, celiac disease and facial asymmetry. Further research is clearly required both to study associations between autoimmune diseases and facial asymmetry and the link between autoimmune diseases and facial asymmetry.
  • Küçük Resim Yok
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    Type 1 Diabetes Mellitus Associated with Autoimmune Thyroid Disease, Celiac Disease and Facial Asymmetry
    (Modestum Ltd, 2014) Akyurek, Nesibe; Atabek, Mehmet Emre; Eklioglu, Beray Selver; Yuca, Sevil Ari
    Patients with type 1 diabetes mellitus are at a great risk of developing other autoimmune diseases. Ten -year-old girl was brought to our clinic with complaints of polydipsia, polyuria and weight loss and was diagnosed as diabetic ketoacidosis due to autoimmune type 1 DM. On physical examination, on the left side of her face mild facial asymmetry was noticed. She had the asymmetry since the birth. Elevated thyroid antibodies associated with diffuse goiter and hypothyroidism led to the diagnosis of autoimmune thyroid disease, and elevated antiendomysial antibodies, anti-gliadin antibodies and abnormal intestinal biopsy findings led to the diagnosis of celiac disease. To our knowledge, this is the first report on a child with a combination type 1 diabetes mellitus, autoimmune thyroid disease, celiac disease and facial asymmetry. Further research is clearly required both to study associations between autoimmune diseases and facial asymmetry and the link between autoimmune diseases and facial asymmetry.