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  1. 31341
    “…CASE PRESENTATION: A Sri Lankan girl presented with recurrent episodes of jaundice. …”
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    Dubin–Johnson syndrome and intrahepatic cholestasis of pregnancy in a Sri Lankan family: a case report
  2. 31342
    “…The proband is a 4-years-old girl with acute onset of focal numbness and weakness in her right hand. …”
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    Hereditary neuropathy with liability to pressure palsy (HNPP): report of a family with a new point mutation in PMP22 gene
  3. 31343
    “…CASE PRESENTATION: Three and a half years old girl was referred for evaluation of progressive loss of gross motor milestones over 6 months and acute episode of paralysis. …”
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    A child with distal (type 1) renal tubular acidosis presenting with progressive gross motor developmental regression and acute paralysis
  4. 31344
    “…CONCLUSIONS: Totally endoscopic operation for ASD closure on beating heart is safe, with short recovery period, and surgical scars are of high cosmetic value, especially in a woman and girl.…”
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    Totally Endoscopic Cardiac Surgery for Atrial Septal Defect Repair on Beating Heart Without Robotic Assistance in 25 Patients
  5. 31345
    “…CASE PRESENTATION: A 3.5 year old girl presented with repeated hypoglycaemic myoclonic events. …”
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    “Crying without tears” as an early diagnostic sign-post of triple A (Allgrove) syndrome: two case reports
  6. 31346
    “…PATIENT CONCERN: A 27-month-old girl was first referred for a mediastinal lesion found incidentally on a chest radiograph. …”
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    Foregut duplication cyst: a novel computed tomography finding mimicking a small bowel hernia: A case report
  7. 31347
    “…CASE PRESENTATION: A 10-year-old girl of Moroccan origin presented to our institution for genetic consultation for genetic testing of the MEFV gene. …”
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    A novel single variant in the MEFV gene causing Mediterranean fever and Behçet’s disease: a case report
  8. 31348
    “…CASE PRESENTATION: Our patient is a 2-year-old white girl from the first pregnancy of a non-consanguineous healthy young white couple (father 33-years old and mother 29-years old). …”
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    16p11.2 microdeletion syndrome: a case report
  9. 31349
    “…The patient achieved a complete resolution of all symptoms with pulse methylprednisolone followed by oral prednisone. A 4-year-old girl with cystic fibrosis, pancreatic insufficiency, chronic pulmonary colonization by Gram-positive bacteria admitted for pulmonary exacerbation was treated with intravenous piperacillin-tazobactam and tobramycin. …”
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    Drug reaction with eosinophilia and systemic symptoms (DRESS) syndrome in two young children: the importance of an early diagnosis
  10. 31350
    “…CASE PRESENTATION: Here we described a girl in a consanguineous Jordanian family with abnormal facial appearance and postnatal growth delay. …”
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    Novel frame shift mutation in ERCC6 leads to a severe form of Cockayne syndrome with postnatal growth failure and early death: A case report and brief literature review
  11. 31351
    “…PATIENT CONCERNS: An 11-year-old girl who was a climber complained of pain on her left wrist without direct trauma. …”
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    Physeal fracture in the wrist and hand due to stress injury in a child climber: A case report
  12. 31352
    “…PATIENT CONCERNS: The patient was a 17-year-old girl with growth retardation, hearing loss, and severe skeletal dysplasia(scoliosis and chicken breast), and was evaluated to have normal nervous system function and intelligence by physicians. …”
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    Analysis of endocrine hormone metabolism level in a Chinese patient with mucopolysaccharidosis IVA: A case report
  13. 31353
    “…CASE PRESENTATION: A Caucasian 13-year-old girl underwent measurement of best corrected visual acuity, ophthalmoscopic evaluation, and fundus autofluorescence examination. …”
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    Swept source optical coherence tomography and optical coherence tomography angiography in pediatric enhanced S-cone syndrome: a case report
  14. 31354
    “…CASE PRESENTATION: A six-month-old girl with persistent high fevers was found to have pyuria and bacteriuria. …”
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    A case report of infantile cystic nephroblastoma
  15. 31355
    “…The first patient is a 6-year-old girl who presented to the emergency department in anaphylaxis (urticaria and respiratory symptoms) minutes after inhaling powdered American ginseng. …”
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    First-reported pediatric cases of American ginseng anaphylaxis and allergy
  16. 31356
    “…CASE PRESENTATION: We describe a 13-year-old Japanese girl with a history of recurrent hepatic impairment, which had not been thoroughly investigated. …”
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    Gallbladder agenesis with hepatic impairment: a case report
  17. 31357
    “…PATIENT CONCERNS: An 11-year-old girl presented to our hospital with severe lower abdominal pain, lower vaginal atresia with enlargement of the upper vagina and a bicornuate uterus with a Y-shaped uterine cavity filled with hematometra on pelvic magnetic resonance imaging. …”
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    Congenital anal atresia with rectovestibular fistula, scoliosis, unilateral renal agenesis, and finger defect (VACTERL association) in a patient with partial bicornuate uterus and distal vaginal atresia: A case report
  18. 31358
    “…PATIENT CONCERNS: A 26-month-old girl with a history of fever and lethargy for 3 days and intermittent seizures for 2 hours associated with rash on 4 limbs was brought to a hospital. …”
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    Pathologic and molecular studies of enterovirus 71 infection in a fatal case from a recent epidemic in China: A case report
  19. 31359
    “…A c.6954 + 3A > C substitution and a c.5862 + 1delG deletion were identified, one of each, in a 6 year-old boy and 39 month-old girl. Further studies confirmed that both variants introduce premature termination codons, resulting in the formation of truncated proteins p.…”
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    Molecular characterization of two novel intronic variants of NIPBL gene detected in unrelated Cornelia de Lange syndrome patients
  20. 31360
    “…CASE PRESENTATION: A misdiagnosed ten-and-a-half-year-old girl with osteoid osteoma involving the distal phalanx of a little finger is presented. …”
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    Unusual localization and presentation of osteoid osteoma mimicking juvenile spondyloarthritis: a case report
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