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  • image/svg+xml art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos Open Access logo, converted into svg, designed by PLoS. This version with transparent background. http://commons.wikimedia.org/wiki/File:Open_Access_logo_PLoS_white.svg art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos http://www.plos.org/
    Authors: ARUN, Funda;

    Various hypno-sedative and analgesic drugs are available in the setting of pediatric procedural sedation and analgesia outside the operating room. The aim was to perform a systematic internet based literature review to investigate sedative drug choices and associated clinical outcomes in pediatric population.

    image/svg+xml art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos Open Access logo, converted into svg, designed by PLoS. This version with transparent background. http://commons.wikimedia.org/wiki/File:Open_Access_logo_PLoS_white.svg art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos http://www.plos.org/ Pediatric Practice a...arrow_drop_down
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  • image/svg+xml art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos Open Access logo, converted into svg, designed by PLoS. This version with transparent background. http://commons.wikimedia.org/wiki/File:Open_Access_logo_PLoS_white.svg art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos http://www.plos.org/
    Authors: AYAS, Şule; ÖZTÜRK, Kezban; GENÇELİ, Mustafa; ÇAKSEN, Hüseyin;

    Introduction: Phenytoin is an aromatic ring antiepileptic drug (AED) commonly used in epilepsy. As well as the side effects such as phenytoin-induced Steven-Johnson syndrome, DRESS (Drug Reaction with Eosinophilia and Systemic Symptoms) and cerebellar toxicity, a rarely life-threatening anaphylaxis requiring urgent treatment can be seen.

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      image/svg+xml art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos Open Access logo, converted into svg, designed by PLoS. This version with transparent background. http://commons.wikimedia.org/wiki/File:Open_Access_logo_PLoS_white.svg art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos http://www.plos.org/
  • image/svg+xml art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos Open Access logo, converted into svg, designed by PLoS. This version with transparent background. http://commons.wikimedia.org/wiki/File:Open_Access_logo_PLoS_white.svg art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos http://www.plos.org/
    Authors: KASAP, Tuba; AYKAN, Hakan; KARAGÖZ, Tevfik;

    Kalp yetmezliği klinik bir sendrom olup kalbin, vücudun metabolik ihtiyaçlarını karşılayamaması olarak tanımlanmaktadır. Bu tablo acil tedavi gerektiren yüksek riskli bir durum olduğundan tanı ve tedavideki gecikmeler mortalite ve morbiditede artışa neden olmaktadır. Bu derlemede çocuklarda kalp yetmezliğinin etyolojisi, klinik belirtileri üzerinde durulmuş ve tanısal tetkikler tartışılmıştır. Anahtar kelimeler: Çocuk, kalp yetmezliği, tanı.

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    Authors: ERDEN, Semih;

    Bruxism related to sleep involves activation of the chewing muscles and results in tooth clenching, chattering, and grinding. Risk factors related to bruxism in sleep are obstructive sleep apnea, alcohol, caffeine, parasomnias such as sleep-talking and sleepwalking, anxiety, and other psychiatric and neurologic disorders, and some medications. There is still no treatment proven to be effective for the treatment of sleep bruxism. This case presents three school-aged children who presented with bruxism who responded to low-dose melaton

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    Authors: Hasan Bozkurt; Seda Tabak; Serkan Şahin;

    Bu yazıda distoni tedavisi için parenteral olarak verilen biperiden sonrası deliryum tablosu gelişen bir çocuk olgunun sunulması amaçlanmıştır. Olgumuz yazında çocuk yaşta biperiden ile ilişkili ilk deliryum olgusudur.

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  • image/svg+xml art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos Open Access logo, converted into svg, designed by PLoS. This version with transparent background. http://commons.wikimedia.org/wiki/File:Open_Access_logo_PLoS_white.svg art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos http://www.plos.org/
    Authors: EĞİL, Oğuz; AKÇAY, Memduha; OLTULU, Pembe; PEKCAN, Sevgi;

    In chronic cough, one of the etiologies is microaspirations due to gastroesophageal reflux diseases. “Lipid-laden macrophage” (LLM) the definition of lipid-containing macrophage after staining with Sudan 4 or Oil Red O. It is considered as a sign of gastroesophageal reflux in recurrent pneumonia. Materials and MethodsIn this study, we retrospectively evaluated the children undergoing bronchoscopy between 2016 and 2019 in our center. Patients’ medical records have been retrospectively analyzed and their parents were called for further information

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    Authors: MISIRLIOĞLU, Merve; DİLEK, Mustafa;

    İntrauterin dönemde ultrasonografinin sık kullanılması sonucu, fetal anatominin ayrıntılı değerlendirilebilmesi nedeniyle, intrauterin kistlerin tanı insidansı artmaktadır. Bu nedenle fetal ve neonatal over kistlerinin tespiti ve tedavisinde yakın perinatal takip önemlidir. Kistin boyutuna ve içeriğine, gelişen komplikasyonlara göre tedavisi planlanmaktadır. Bu vaka sunumda antenatal tanı alan ve postnatal intestinal obstruksiyona neden olması nedeniyle ooferektemi ve over kist eksizyonu yapılan yenidoğan sunulmuştur.

    image/svg+xml art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos Open Access logo, converted into svg, designed by PLoS. This version with transparent background. http://commons.wikimedia.org/wiki/File:Open_Access_logo_PLoS_white.svg art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos http://www.plos.org/ Pediatric Practice a...arrow_drop_down
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    Authors: KÖKER, Nezihe;

    Leucocyte adhesion deficiency disease is a type of immunodeficiency resulted as loss of function to reaction to infectious disease, pus formation, disrupted wound healing. Here we report two LAD1 and two LAD3 with their clinical and functional analysis. 3 of 4 patients are Syrian origin and born into consanguineous families. Their diagnosis are made by flow cytometry and due to high leucocyte count. LAD3 patients have normal CD11abc CD18 levels so they’re diagnosed by adhesion assay.Both confirmed with genetical mutations on ITGB2 and FERMT3. 3 of 4 underwent successful HSCT but one is unfortunately passed away.

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    Authors: GÜRHAN, Gülüzar; ATAŞ, Bülent; PİŞKİN, Mesut;

    Urofacial syndrome (US) or Ochoa syndrome is a syndrome characterized by presence of neurogenic bladder (NB) in absence of a neurological abnormality and mechanical obstruction, as well as by a characteristic facial appearance. As the micturition/urine storage center, laughing and crying centers and origin of the facial nerve are in close proximity in the reticular formation, crying facial expression when laughing and clinical presentation of NB are observed. In this manuscript a case who presented with incontinence, was noticed to have crying facial expression when laughing and, unfortunately, developed chronic renal failure (CRF) due to NB is reported.

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    Authors: BAŞ, Melike; MOLU, Birsel; BÜKÜLMEZ, Ayşegül;

    The aim of this study is to help nursing care and the importance of emotional support in coping process of a child with T1DM and CD. It is evaluated with nursing model based on Roy adaptation model. Seventeen years old female patient was admitted to a university hospital with the diagnosis of T1DM + CD. The patient also had anxiety. It was determined that the patient had eating disorder and did not use his insulin regularly. As seen in this case, it is important to provide emotional support in coping with anxiety and fear of unknownness in a new disease.

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    Authors: GÜLTEKİN, Ümit; TOKGÖZ, Hüseyin;

    Vitamin B12 (cobalamine) deficiency is one of the nutritional deficiencies in children. It can also be seen in infants whose mothers have nutritional deficiency. The involuntary movements is known to be associated with vitamin B12 deficiency. But also this type of movements can be seen in the patients who are on vitamin B12 tretament. We present a patient who had involuntary movements after enteral vitamin B12 treatment, on which reported cases are rarer than parenteral administration. We want to emphasize continuation of treatment is much more important than these involuntary movements observed temporarily.

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    Authors: ÜNAL, Emin; OFLAZ, Mehmet Burhan; YILMAZ, Hüseyin; ŞAP, Fatih; +1 Authors

    Pericardial cysts are smooth-walled congenital benign cysts which are unilocular with an external wall comprised of mesothelial or endothelial cells. They account for 6-7% of all mediastinal lesions. They are usually found in the costophrenic angle. Although they are generally asymptomatic, up to 20% of the patients may have nonspecific symptoms. PA chest x-ray, echocardiography and CT are the most commonly used diagnostic methods. Diffusion-weighted MRI has also been suggested. Surgical excision is at the forefront in treatment, being performed with low morbidity and mortality rates. In cases for which a surgery cannot be performed, complications such as hemorrhage, spontaneous rupture of the cyst or infected cyst may develop.

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    Authors: ESME, Hıdır; DOĞAN, Hasan;

    Although corrosive injury of the digestive tract is a well-known clinical entity, damages of the airway, a critically life-threatening condition, has not been clearly documented. Tracheal stenosis is very rare associated with corrosive acid ingestion. We report the case of a 4-year-old girl child who presented to the emergency department three week after accidentally drinking an acidic cleaning agent stored in unlabeled bottle. Rigid bronchoscopy was carried out to observe the stenosis. She was treated by serial dilation, repair of tracheal laceration, and placement of a temporary polyurethane-coated nitinol stent. Careful and accurate stent placement may provide significant and life-saving airway improvement as observed in the presenting pediatric case.

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    Authors: Bethany Slater; Andrea Sotelo;

    There are a number of causes of small bowel obstruction in infants, most commonly from congenital causes. Inflammatory myofibroblastic tumor (IMT) of the alimentary tract is a very unusual cause of intestinal obstruction in children. IMT is a rare, benign solid tumor that presents mostly in the pediatric population. We present a case of a jejunal IMT causing bowel obstruction in a four month old female treated with laparoscopic resection and bowel anastomosis.

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    Authors: ÖZCAN SIKI, Fatma; SEKMENLİ, Tamer;

    In our institution, we describe 2 children (5,15 years old) with acute appendicitis in case of SARS-CoV-2 infection and we suggest a possible relationship. We think that testing for this infection is necessary in patients with a history of contact with a person with SARS-CoV-2 infection and severe gastrointestinal symptoms. Kurumumuzda SARS-CoV-2 enfeksiyonu durumunda akut apandisitli 2 çocuğu (5,15 yaş) tanımlıyoruz ve olası bir ilişki olduğunu düşündürüyoruz. SARS-CoV-2 enfeksiyonlu kişi ile temas öyküsü olan ve şiddetli gastrointestinal semptomları olan hastalarda bu enfeksiyon için test yapmanın gerekli olduğunu düşünmekteyiz.

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    Authors: Mine Akın;

    Çocuklarda laparoskopi önceleri tanısal amaçla uygulanmaya başlanmış, ancak o dönemde non-invaziv görüntüleme yöntemlerinin gelişmesinden dolayı geri planda kalmıştır. Erişkin hastalarda laparoskopinin operatif morbiditeyi ve hastanede kalış süresini azaltmada katkı sağladığı farkedilince pediyatrik hastalarda da tedavi amaçlı kullanımı yaygınlaşmıştır. Açık cerrahide olmayan bazı özellikler laparoskopik ameliyatlarda anestezi yönetiminin rolünü ve önemini arttırmaktadır.

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    Authors: ATAŞ, Bülent; PİŞKİN, Mesut;

    Tethered Cord syndrome (TCS) is a disease in which neural tissue ischemia develops as a result of stretching of the spinal cord and eventually progressive neurological loss develops. Children with TCS have urinary day-night incontinence, frequent urination and frequent urinary infection. Signs and symptoms can be present from birth, but often occur over time. The feared condition is renal damage due to neurogenic bladder (NM) and chronic renal failure (CRF). In this article, we present a 14-year-old female patient who developed CRF due to TCS, who had leaked urine during day and night since her childhood and later presented with renal failure.

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    Authors: ERGANİ, Anna Carina; GÜMÜŞ, Meltem; SEKMENLİ, Dr.tamer; EMİROĞLU, Halil Haldun;

    Gastrointestinal kanamalar çocukluk çağında sık karşılaşılan morbidite ve mortalite nedenleriden biridir. Gastrointestinal kanalda Treitz ligamanının proksimalinden olan kanamalar üst gastrointestinal sistem kanamaları olarak adlandırılır. Aksine Treitz ligamanının distalinden olan kanamalar ise alt gastrointestinal sistem kanamaları olarak adlandırılmaktadır.Bu yazıda kanlı dışkılama nedeni ile başvuran çocuğa tanısal yaklaşım gözden geçirilmektedir. Hemorrhages from the proximal of the Treitz ligament in the gastrointestinal tract are called upper gastrointestinal system hemorrhages. On the contrary, bleeding from the distal of Treitz ligament is called lower gastrointestinal bleeding.In this case report, the diagnostic approach to the child who presented with bloody defecation is reviewed.

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    Authors: SARIKAYA, Mehmet; SARIKAYA, Sevcan;

    İmperfore himen nadir görülen bir konjenital anomalidir. Ergenlik dönemine kadar farkedilmeleri oldukça zordur. Sıklıkla periyodik karın ağrısı, karında kitle, idrar yapamama, primer amenore gibi semptom ve bulgularla kendini gösterir. 12 yaşında bir imperfore himen-hematokolpos birlikteliği olgusunu sunmaktayız. Karın ağrısı, idrar yapamama ve karında şişlik şikayetiyle tarafımıza başvuran hastanın fizik muayenesinde himenin imperfore olduğu görüldü. Hastaya çekilen batın ultrasonunda hematokolpos tespit edildi. Hastaya genel anestezi altında himenotomi uygulandı.İmperfore himen, periyodik karın ağrısı, karında kitle, primer amenore ve idrar yapamama ile başvuran hastalarda mutlaka akılda tutulması gereken nadir bir konjenital anomalidir.

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    Authors: İLİK, Durmuş Ali; KESEN, Nur Feyzal;

    Bu çalışmada, bağlanma ve aile aidiyeti kavramlarının bazı değişkenlerle farklılaşıp farklılaşmadığına ve arasındaki ilişkiye bakılması amaçlanmıştır. Kahramanmaraş İli Elbistan ilçesinde Lise düzeyinde eğitim gören kişilere, bağlanma ve aile aidiyetlerini ölçmek üzere araştırmacılar tarafından hazırlanan anket ve ölçekler uygulanmıştır.Nicel araştırma tasarımlarından tarama yöntemi kullanılmıştır. Çalışma sonucunda lise öğrencilerinin saplantılı bağlanma ve aile aidiyeti arasında negatif anlamlı bir ilişki bulunmuştur. Ayrıca kardeş sayısı arttıkça aile aidiyeti düşmektedir. Erkeklerin saplantılı bağlanmaları ve güvenli bağlanma stilleri daha yüksek iken kızların korkulu bağlanmaları ve kendilik aidiyeti puan ortalamaları daha yüksek çıkmıştır

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    Authors: KALECİ, Elanur; GEÇKİL, Emine;

    Type 1 Diabetes Mellitus (DM) is a chronic metabolic disease caused by beta-cell destruction due to autoimmune or other causes and resulting from absolute insulin deficiency. Type 1 diabetes is most commonly seen in children and adolescents. Because adaptation to diabetes leads to changes in the life style of the child and family, adaptation to the disease is quite difficult.Type 1 diabetes mellitus has many psychosocial effects (anxiety, fear, anxiety, mourning, anxiety) on children. In this review, we aimed to investigate the psychosocial adaptation of children and their families with Type 1 diabetes mellitus. CONCLUSION: Psychosocial evaluation, counseling and education services of children and their families diagnosed with type 1 diabetes should be provided. Thus, adaptation of the child and family to the disease will be ensured, complications will be prevented and quality of life will be improved.

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    Authors: KÖKER, Mustafa Yavuz;

    Recurrent bacterial and fungal infections that involve the lungs, lymph nodes, liver and other visceral organs. Granuloma formation may occur in the tissues of the infection area, depending on the prolongation of infections in KGH. Hypergammaglobulinemia (IgG ), hepato-splenomegaly and enteritis are frequently observed. The X-CGD form, which is seen especially in boys, usually appears before the age of 1 and is more severe. Mild phenotypes, especially autosomal recessive form (p47-phox deficiency) may occur at a later age. The patient and healthy neutrophil population, which constitute the carrier character in mothers in X-linked form, are observed. Mild clinical signs can be observed in approximately 50% of mothers. In some rare cases, CGD symptoms can be observed in women due to x-ch inactivation deviation.

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    Authors: VATANSEV, Hülya;

    About a quarter of the word’s population is infected with Mycobacterium tuberculosis, but this bacterium causes tuberculosis in less than 10% of infected individuals. In the countries in wich tuberculosis is highly endemic, primary tuberculosis is particulary common in the children and adults. Clinical and epidemiological studies suggest that tuberculosis in humans has a strong genetic basis. Autosomal recessive (AR) complete interleukin-12 receptor β 1 (IL-12R β 1) and tyrosine kinase 2 (TYK2) deficiencies are the only two inborn errors of immunity reported to date to underlie primary tuberculosis in otherwise healthy patients in two or more kindreds (1,2). Inherited IL-12R β 1 and TYK2 deficiencies impair both IL-12– and IL-23–dependent IFN-g immunity and are rare also causes of tuberculosis (3,4).

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