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  1. 31581
    “…CASE REPORTS: A 4-year-old girl presented with pruritic, erythematous lesions on the head with alopecia. …”
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    A Household Microsporum canis Dermatophytosis Suggested by Matrix-Assisted Laser Desorption/ Ionization Time-Of-Flight Mass Spectrometry Analysis
  2. 31582
    “…CASE SUMMARY: A 2-year-old girl diagnosed with ornithine transcarbamylase deficiency required liver transplantation. …”
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    Cholangiojejunostomy for multiple biliary ducts in living donor liver transplantation: A case report
  3. 31583
    “…RESULTS: Among the total of 525 pupils, 24 (4.6%) were found to have ADHD symptom types (boy: 6.5%; girl: 2.1%). The combined ADHD type accounted for the highest proportion of 3.4%, followed by predominantly inattentive and predominantly hyperactivity type. …”
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    Attention Deficit Hyperactivity Disorder (ADHD) and Associated Factors Among First-Year Elementary School Students
  4. 31584
    “…We report a 13-year-old girl of Chinese Han ethnicity with arthralgia and fracture as initial symptoms of WD. …”
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    Osteoarticular manifestations as initial symptoms of WD with novel compound heterozygote mutations in the ATP7B gene: a case report
  5. 31585
    “…We present an interaction analysis of a single case study of the first 20 min of a child therapy session with an adopted girl aged 4 years brought to treatment because of “unexplainable rage.” …”
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    Doing Contrariness: Therapeutic Talk-In-Interaction in a Single Therapy Session With a Traumatized Child
  6. 31586
    “…Paroxysmal movements, other transient neurological disorders, or hemiplegic events can occur in GLUT1-DS patients with a mild phenotype. Case: We report on a girl with GLUT1-DS, due to SLC2A1 mutation, with a mild phenotype. …”
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    CACNA1A-Linked Hemiplegic Migraine in GLUT 1 Deficiency Syndrome: A Case Report
  7. 31587
    “…Inclusion criteria in this study were the target population of women and girl and descriptive and qualitative studies on waterpipe use among women. …”
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    Determinants of Waterpipe Smoking Among Women: A Systematic Review
  8. 31588
    “…Refugee adolescents who do not agree that a girl cannot get pregnant if she has sex while standing up (knowledge about getting pregnant) were significantly less associated with sexual behaviour (OR  =  0.30; 95% CI  =  0.10–0.85). …”
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    Adolescent sexual behaviour in a refugee setting in Uganda
  9. 31589
    “…Patient 1, a 2-year-old girl, presented with mild bleeding and was found to have a FVII:C of 0.2% and a compound heterozygous F7 Cys389Gly/Cys115Arg mutation. …”
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    Identification of two novel mutations in three children with congenital factor VII deficiency
  10. 31590
    “…AIM AND OBJECTIVE: The present article aims to describe and discuss the preventive clinical management of a pre-eruptive intracoronal resorption (PEIR) defect on a maxillary right second premolar of an 11-year, 5-month-old girl. BACKGROUND: Pre-eruptive intracoronal resorption is described as an abnormal, well-circumscribed, radiolucent area, occurring within the coronal dentinal tissue close to the dentinoenamel junction of unerupted teeth and extending into various depths of the dentin. …”
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    Management of Maxillary Premolar with Pre-eruptive Intracoronal Resorption: A 5-year Follow-up Case
  11. 31591
    “…CASE DESCRIPTION: A 9-month-old infant girl presented to the Pediatric Dental Department with a swelling over the maxillary alveolar ridge. …”
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    Isolated Focal Infantile Hemangioma of the Alveolar Ridge with Glucose Transporter-1 Reactivity: An Aberrant Presentation
  12. 31592
    “…CASE PRESENTATION: We report the case of a 5-year-old Saudi girl who presented to the pediatric emergency department with fever and new-onset status epilepticus. …”
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    Elevated intracranial pressure requiring decompressive craniectomy in a child with progressive primary angiitis of the central nervous system: a case report
  13. 31593
    “…Our patient was an 11-year-old girl who presented with classic symptoms and signs of PCC/PG and a CT scan of the abdomen that showed a right-sided paravertebral mass. …”
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    Perioperative control of paroxysmal hypertension using esmolol with alpha-blockade in a child with a germline mutated paraganglioma
  14. 31594
    “…CASE REPORT: The patient was a 4-year-old girl with PS, TCS, and abnormal hyperplasia of non-fused intrapulmonary cartilages. …”
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    Autopsy Case of Pfeiffer Syndrome Type 2, a Phenotype of Fibroblast Growth Factor Receptor-Associated Craniosynostosis Syndromes, with Tracheal Cartilage Sleeve and Abnormal Hyperplasia of Bronchial Cartilages
  15. 31595
    “…CASE PRESENTATION: We report on a girl, 4 years old, of consanguineous parents, with a 15q26 deletion. …”
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    15q26 deletion in a patient with congenital heart defect, growth restriction and intellectual disability: case report and literature review
  16. 31596
    “…Case Report and Methods: We report the case of a 16-year-old girl with multiorgan sarcoidosis and renal involvement. …”
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    Case Report: Pediatric Renal Sarcoidosis and Prognostic Factors in Reviewed Cases
  17. 31597
    “…CASE PRESENTATION: A 13-year-old girl with chronic kidney disease (CKD) stage 5D, on continuous cycling PD (CCPD) for 8 years, presented with cloudy PD effluent, with no abdominal discomfort or fever. …”
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    Peritoneal dialysis-related peritonitis caused by Gordonia bronchialis: first pediatric report
  18. 31598
    “…In this case report, we report a pediatric patient with COVID-19 and atypical hemolytic uremic syndrome (aHUS). A 3-year-old girl with fever and respiratory distress was admitted to the hospital. …”
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    Thrombotic Microangiopathy in a Severe Pediatric Case of COVID-19
  19. 31599
    “…CASE REPORT: A 22-month-old girl presented to our primary care clinic in Selangor, Malaysia with abnormal gait and bowing of the legs during the COVID-19 pandemic. …”
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    Rickets Due to Severe Vitamin D and Calcium Deficiency During the COVID-19 Pandemic in Malaysia
  20. 31600
    “…CASE PRESENTATION: A 16‐year‐old Mongolian girl approached our clinics with retinal detachment. …”
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    Case report of the first molecular diagnosis of Stickler syndrome with a pathogenic COL2A1 variant in a Mongolia family
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