Person: CESUR, YAŞAR
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Publication Metadata only ASSOCIATION OF PULMONARY HEMOSIDEROSIS AND CELIAC DISEASE(2011-05-01T00:00:00Z) Dogan, Murat; Bektas, Mehmet Selcuk; Dogan, Sekibe Zehra; Aktar, Fesih; Cesur, Yaşar; CESUR, YAŞARIdiopathic pulmonary hemosiderosis (IPH) is a rare disease of unknown autoimmune etiology mainly affecting children and adolescents. We report the case of an 6-years-old boy with cough and tiredness. There were no gastrointestinal symptoms were not determined. Body weight and height were in normal percentiles. Physical examination revealed cutaneous and mucosal pallor, due to severe anemia (hemoglobin 3 g/dL). Infiltrations were seen at the chest X-rays at both lungs, but markedly at left lung. In sputum examinations, hemosiderin-laden macrophages were seen. The diagnosis of IPH was made. The association of IPH and Celiac disease (CD) is well known. Searching associated CD was performed and then confirmed by biological and histological examinations. A gluten-free diet was initiated. Evolution was favorable. Searching for CD in IPH should be done, even in the absence of gastrointestinal symptoms.Publication Metadata only CONGENITAL HYPOTHYROIDISM WITH ISOLATED FIBULA AGENESIS(2010-05-01T00:00:00Z) Dogan, Murat; Yilmaz, Cahide; Caksen, Hueseyin; Cesur, Yaşar; Akpinar, Fuat; Gueven, Ahmet Sami; CESUR, YAŞARAlthough congenital hypothyroidism is seen often as an isolated case, it can also be seen as a part of some syndromes like Schinzel-Giedion, Aicardi-Goutieres-like, cleidocranial dysplasia and deletion of 18q. It is also well known that congenital hypothyroidism may be associated with other congenital malformations, especially with cardiac heart diseases, skeletal abnormalities, Central nervous system and eye malformations. In this article, 11-years-old-girl with fibula agenesis associated with congenital hypothyroidism because of thyroid gland hypoplasia is presented. In our knowledge, both congenital hypothyroidism and isolated fibula agenesis have not been published before in the literature.Publication Metadata only The Relationship Between Precocious Puberty and Premature Thelarche with Serum Irisin Levels(2019-09-01T00:00:00Z) Özgen, İlker Tolga; Kutlu, Esra; Bulut, Huri; Temur, Hafize Otcu; Torun, Emel; Cesur, Yaşar; KUTLU, ESRA; ÖZGEN, İLKER TOLGA; BULUT, HURI; TORUN, EMEL; CESUR, YAŞARhttps://www.karger.com/?DOI=10.1159/000495021Publication Metadata only Celiac disease with celiac crisis Çöliak kriz ile seyreden çöliak hastalıǧı(2010-01-01T00:00:00Z) Dogan, Murat; Yuca, Sevil Ari; Acikgöz, Mehmet; Doǧan, Sekibe Zehra; Kaya, Avni; Cesur, Yaşar; CESUR, YAŞARPublication Metadata only Hypernatremia in hospitalized children(2017-01-01T00:00:00Z) Yuca, Sevil; Cesur, Yaşar; Caksen, Huseyin; Arslan, Derya; Yilmaz, Cahide; Kaya, Avni; CESUR, YAŞARObjective: Hypernatraemia has serious complications such as brain injury, brain oedema and seizure. In this study, the incidence among children hospitalized hypernatremia, causes, development time, clinical features, and morbidity, and aimed to reveal the effect on mortality.Publication Metadata only Rickets in healthy adolescents in Van, the eastern of Turkey(2010-12-23T00:00:00Z) Üner, Abdurrahman; Acar, Mehmet Nuri; Cesur, Yaşar; Doǧan, Murat; Çaksen, Hüseyin; Temel, Hayrettin; Sal, Ertan; Özbek, Hanef; CESUR, YAŞARPublication Metadata only LATE ONSET ARGININE SUCCINATE LYASE DEFICIENCY WITH NORMAL PLASMA AMMONIA LEVEL(2011-01-01T00:00:00Z) Yilmaz, Cahide; Dogan, Murat; Cesur, Yaşar; Caksen, Huseyin; Yuca, Sevil Ari; Atas, Bulent; Tuncer, Oguz; CESUR, YAŞARArginine succinate lyase (ASL) deficiency is one of the most common cause of urea cycle defect and shows all characteristics of this disorders. This disease is presented with hyperammonemia, abnormally kinky hair and mental retardation. 6-years-old-girl was brought to our hospital because of skin eruption, weight loses, abdominal pain, having no appetite, polydipsia and pollakiuria. In physical examination, especially occipital balding, mental retardation, hepatomegaly, ataxia and articulation defect were found. She, who was diagnosed as ASL deficiency after the laboratory examinations, had normal blood ammonia levels. Finally in this study, we emphasize; ASL deficiency must be thought when a child has mental retardation and cerebellar ataxia, even if normal ammonia levels.