Person:
KUTLU, ESRA

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Kurumdan Ayrılmıştır
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ESRA
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KUTLU
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Now showing 1 - 5 of 5
  • PublicationOpen Access
    Pseudohypoparathyroidism Type Ia with Normocalcemia
    (2019-04-01T00:00:00Z) Kutlu, Esra; CESUR, Yaşar; ÖZGEN, İLKER TOLGA; Yesil, Gozde; KUTLU, ESRA; ÖZGEN, İLKER TOLGA; CESUR, YAŞAR; YEŞİL, GÖZDE
    Pseudohypoparathyroidism (PHP) is a heterogeneous group of disorder with parathormone target organ resistance, characterized by hypocalcemia, hyperphosphatemia and high blood parathormone (PTH). Typical phenotypic symptoms and additional hormonal resistance can be observed in type Ia, which is also known as Albright hereditary osteodystrophy. Our patient was an eight-year and nine-month old girl with typical Albright-s hereditary osteodystrophy phenotype including short stature, obesity, round face, low nasal bridge, shortened metacarpals, and mild mental retardation. In her biochemical examination, high PTH level and hypothyroidism is detected in spite of normal calcium and phosphor levels. As a result of clinic and laboratory tests, the findings were consistent with PHP type Ia with normocalcemia. In her guanine nucleotide binding protein (G protein), alpha stimulating activity polypeptide 1 (GNAS 1) gene serial analysis, C-308T>C (p1103T) transformation was detected, which was previously reported in a PHP type Ia patient. In this report, we-ve aimed to emphasize the fact that calcium and phosphor level in the blood of the patient with PHP type Ia can be measured normal.
  • PublicationMetadata only
    Tiroid hormone direnci olan iki olgu
    (2017-04-30) CESUR, YAŞAR; KUTLU, ESRA; ÖZGEN, İLKER TOLGA; YEŞİL, GÖZDE; CESUR, YAŞAR; KUTLU, ESRA; ÖZGEN, İLKER TOLGA; YEŞİL, GÖZDE
  • PublicationMetadata only
    Normokalsemik seyreden psödohipoparatiroidi tip 1A
    (2016-10-09) ÖZGEN, İLKER TOLGA; KUTLU, ESRA; YEŞİL, GÖZDE; CESUR, YAŞAR; DUMAN, NİLGÜN; ÖZGEN, İLKER TOLGA; KUTLU, ESRA; YEŞİL, GÖZDE; CESUR, YAŞAR; DUMAN, NİLGÜN
  • PublicationMetadata only
    Laron sendromu
    (2016-10-09) KUTLU, ESRA; ÖZGEN, İLKER TOLGA; YEŞİL, GÖZDE; OĞUR, MUSTAFA; CESUR, YAŞAR; KUTLU, ESRA; ÖZGEN, İLKER TOLGA; YEŞİL, GÖZDE; OĞUR, MUSTAFA; CESUR, YAŞAR
  • PublicationMetadata only
    46XY Cinsel Gelişim Bozukluğunun Nadir Nedeni: 17?-hidroksilaz Eksikliği
    (2017-04-30) CESUR, YAŞAR; ÖZGEN, İLKER TOLGA; KUTLU, ESRA; YEŞİL, GÖZDE; CESUR, YAŞAR; ÖZGEN, İLKER TOLGA; KUTLU, ESRA; YEŞİL, GÖZDE