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  1. 31461
    “…CASE SUMMARY: We report a 4-year-old girl with left hemiparesis after an acute ischemic stroke. …”
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    Idiopathic steno-occlusive disease with bilateral internal carotid artery occlusion: A Case Report
  2. 31462
    “…CASE REPORT: A 17-year-old girl was treated with carbimazole since the age of 15 for hyperthyroidism secondary to Graves’ disease. …”
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    Severe Neutropenia and Hepatotoxicity After Carbimazole Drug Therapy for Hyperthyroidism in a Pediatric Patient: A Case Report
  3. 31463
    “…Eleven point eight percent (n = 2254) of all school students had some form of refractive error. Girl students were found to have a higher refractive error rate (13.3%) compared to boy students (10.1%) across the schools screened. …”
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    They see, they learn: Pre-COVID-19 prevalence of refractive errors in school children in suburban areas of North India
  4. 31464
    “…in exon 1 of PMS2 in tumor and germline material of a girl with ependymoma. Tumor analysis displayed evidence for ALT and low mutational burden (0.6), PMS2 expression was retained, MSI was low. …”
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    Beyond germline genetic testing - heterozygous pathogenic variants in PMS2 in two children with Osteosarcoma and Ependymoma
  5. 31465
    “…RESULTS: The proband, a 4-month-old girl, presented with seizure episodes and mild cardiac hypertrophy and was diagnosed with primary carnitine deficiency (PCD), with carnitine levels of 5.165 mol/L. …”
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    A report of a pedigree with compound heterozygous mutations in the SLC22A5 gene
  6. 31466
    “…Case 1 describes a 15-year-old girl with a 1.055 Mb deletion of terminal 4p, distal to the recognized critical region of WHS, and a large duplication of 9.6 Mb in size from 4p16.3 to p16.1. …”
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    Genotype-phenotype correlation of deletions and duplications of 4p: case reports and literature review
  7. 31467
    “…DISCUSSION: Our findings described two novel mutations in a girl with LGMDR23, which contributes to the genetic counseling of the family and expands the clinical and molecular spectrums of the rare disease.…”
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    Limb girdle muscular dystrophy 23 caused by compound heterozygous mutations of LAMA2 gene
  8. 31468
    “…Here, we report the case of a girl with right body asymmetry, which suggested BWS spectrum. …”
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    Case report: a typical Silver-Russell syndrome patient with hand dystonia: the valuable support of the consensus statement to the wide syndromic spectrum
  9. 31469
    “…CLINICAL CASE: An 11-day-old girl born small for gestational age presented with deterioration of well-being and weight loss. …”
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    Case Report: Severe McCune–Albright syndrome presenting with neonatal Cushing syndrome: navigating through clinical obstacles
  10. 31470
    “…As an illustrative case, we report on a 2-year-old girl who presented a cardioembolic right middle cerebral artery stroke with subsequent malignant edema and ongoing cerebral transtentorial herniation in the course of a severe myocarditis requiring ECMO support. …”
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    Decompressive hemicraniectomy in pediatric malignant arterial ischemic stroke: a case-based review
  11. 31471
    “…Case: Here we present a case of nine-year-old girl who presented to us with complains of nasal obstruction since 3 months and symptoms of sleep disordered breathing. …”
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    Pediatric Oronasopharyngeal Stricture– A Rare Surgical Complication of Adeno-Tonsillectomy Abstract
  12. 31472
    “…CASE PRESENTATION: A 3-year-old girl was transferred to our center for severe cough, shortness of breath, fatigue and fever. …”
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    Pulmonary hypertension— a novel phenotypic hypothesis of Kabuki syndrome: a case report and literature review
  13. 31473
    “…Our experience of managing a drowned 2-year-old girl with hypothermia (23°C) and cardiac arrest (58 min) prompted this summary using the CAse REport (CARE) guideline to address the question of optimal rewarming procedure in such patients. …”
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    Rewarming Young Children After Drowning-Associated Hypothermia and Out-of-Hospital Cardiac Arrest: Analysis Using the CAse REport Guideline
  14. 31474
    “…CASE PRESENTATION: A 7-month-old girl presented to the emergency department of a nearby hospital because she was suspected to have accidentally swallowed heated tobacco. …”
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    Extraction of a metallic susceptor after accidental ingestion of the heated tobaccostick TEREA™: a case report
  15. 31475
    “…CASE PRESENTATION: We describe the case of a six-year-old otherwise healthy girl, who presented a sudden and complete bilateral vision loss after a one-day fever. …”
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    Central retinal artery occlusion in a young child affected by COVID-19: a first case report
  16. 31476
    “…CASE PRESENTATION: We report a case of secretory breast cancer (SBC), a subtype of TNBC, in an 8-year-old girl from our institution. The child presented with a single mass in the left breast only, with no skin rupture and no enlargement of the surrounding lymph nodes. …”
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    A case report and literature review on a rare subtype of triple-negative breast cancer in children
  17. 31477
    “…Case 2: A 4-month-old girl with a deletion in chromosome 13 was referred for bilateral RB. …”
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    Massive Uveal Relapse of Retinoblastoma Presumed to Be Choroidal Tumorous Involvement: Case Series
  18. 31478
    “…CASE PRESENTATION: We describe a 15-year-old girl with severe weight loss and liver damage whose liver enzymes normalized after 1.5 months of hospitalization and weight gain. …”
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    Iron overload may be critical for liver dysfunction in anorexia nervosa, and the role of haematocrit-adjusted albumin in assessing nutritional status: a case report
  19. 31479
    “…ABSTRACT: Bilious pleural effusion is a rare entity often iatrogenic, following hepatobiliary surgeries and biliary interventions, and has been reported only in a limited number of patients after liver transplantation. A 5‐year‐old girl underwent living donor liver transplantation due to progressive familial intrahepatic cholestasis. …”
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    Nonoperative management of biliopleural fistula following living‐donor liver transplantation: A case report
  20. 31480
    “…CASE PRESENTATION: Here, we combined exome and genome sequencing techniques to identify the precise breakpoints of heterozygous microduplications in the 6q25.3-q27 region and microdeletions in the 2q37.1-q37.3 region in a proband. The 5-year-old girl exhibited a severe form of congenital cranial dysinnervation disorder (CCDD) in addition to skeletal dysmorphism anomalies and severe intellectual disability. …”
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    Exome and genome sequencing to unravel the precise breakpoints of partial trisomy 6q and partial Monosomy 2q
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