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  1. 31861
    “…CASE SUMMARY: We report the case of an 11-year-old Chinese girl with WD that was associated with immune thrombocytopenia (ITP). …”
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    Wilson disease associated with immune thrombocytopenia: A case report and review of the literature
  2. 31862
    “…Case presentation: A 6-year-old girl visited our outpatient clinic as a result of microcephaly and delayed development. …”
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    Two Novel Mutations (c.883-4_890del and c.1684C>G) of WDR62 Gene Associated With Autosomal Recessive Primary Microcephaly: A Case Report
  3. 31863
    “…At a refugee camp in Turkey, one case of serogroup B IMD was reported in a Syrian girl; four cases of serogroup X IMD occurred in an Italian refugee camp among refugees from Africa and Bangladesh. …”
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    Incidence and Prevention of Invasive Meningococcal Disease in Global Mass Gathering Events
  4. 31864
    “…Case Presentation: A 7-year-old girl with T-cell lymphoma, who presented with severe and persistent toe walking, was assessed 10 times over a course of 6 months by both clinical examination (ankle range of motion measurement) and neurophysiological measures (weight distribution between forefoot and hindfoot, postural sway, body posture, and gait). …”
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    Managing Toe Walking, a Treatment Side Effect, in a Child With T-Cell Non-Hodgkin's Lymphoma: A Case Report
  5. 31865
    “…CASE PRESENTATION: We reported a rare case of a 5-year-old girl who presented with abdominal pain, vomiting, recurrent seizures, and coma. …”
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    Fulminant encephalopathy in a child with hyperferritinemic sepsis: a case report
  6. 31866
    “…CASE PRESENTATION: In case 1, a 2-month-old girl experienced sudden intraperitoneal hemorrhage from the middle colic artery with no apparent trauma. …”
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    Two infant cases of intraperitoneal arterial hemorrhage due to a duplication cyst: a case report
  7. 31867
    “…Patient 2: a 12-year-old girl with lipodystrophy phenotype and hypertriglyceridemia detected in the first year of life and abnormalities in the global longitudinal strain, evaluated by speckle-tracking echocardiography last year. …”
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    Leu124Serfs*26, a novel AGPAT2 mutation in congenital generalized lipodystrophy with early cardiovascular complications
  8. 31868
    “…CASE PRESENTATION: This case was a 13-year-old girl. Medical history: She visited the pediatric department with a chief complaint of headache. …”
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    CS-08 A CASE OF CD 57 NEGATIVE OLFACTORY GROOVE SCHWANNOMA IN WHICH SCHWANN / 2 E AND SOX10 WAS USEFUL FOR DISTINGUISHING FROM OEC TUMOR: A CASE REPORT AND REVIEW OF THE LITERATURES
  9. 31869
    “…Twenty patients (80%) were males, and all except 1 girl had unilateral disease. The presenting complaint was impaired vision in 13 (50%) eyes, leukocoria in 6 (23%) eyes, and strabismus in 7 (27%) eyes. …”
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    Coats’ disease: characteristics, management, outcome, and scleral external drainage with anterior chamber maintainer for stage 3b disease
  10. 31870
    “…CASE DESCRIPTION: This is a case report of disulfiram toxicity in a 4.5-year girl who ingested 4–5 tablets of disulfiram (approximately 1–1.25 g) accidentally and presented with hypoglycemia and encephalopathy. …”
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    Acute Disulfiram Poisoning in a Child: A Case Report and Review of Literature
  11. 31871
    “…CASE PRESENTATION: Our patient was a 13-year-old Mestizo girl with an extensive family history of cancer who was diagnosed with anaplastic astrocytoma. …”
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    A deep analysis using panel-based next-generation sequencing in an Ecuadorian pediatric patient with anaplastic astrocytoma: a case report
  12. 31872
    “…In family A, following a brief illness, a 4‐year‐old girl presented comatose with lactic acidosis and multiorgan failure. …”
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    Pathogenic variants in SQOR encoding sulfide:quinone oxidoreductase are a potentially treatable cause of Leigh disease
  13. 31873
    “…Partner readiness to assume responsibility for the girl and the baby was a key consideration in either continuing the pregnancy to term or opting for an abortion. …”
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    Decision-making preferences and risk factors regarding early adolescent pregnancy in Ghana: stakeholders’ and adolescents’ perspectives from a vignette-based qualitative study
  14. 31874
    “…CASE PRESENTATION: A 5-year-old girl with single ventricle physiology was referred to our hospital from Kazakhstan for a Fontan operation. …”
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    Half-turned truncal switch operation after single ventricle palliation in a patient with borderline left heart hypoplasia
  15. 31875
    “…CASE SUMMARY: We report a 7-mo-old girl with cytomegalovirus infection presenting hepatomegaly, jaundice, liver transaminase elevation, fasting hypoglycemia, hyperglycosuria, proteinuria, hypophosphatemia, rickets, and growth retardation. …”
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    Fanconi-Bickel syndrome in an infant with cytomegalovirus infection: A case report and review of the literature
  16. 31876
    “…CASE PRESENTATION: A now-11-year-old girl presented in early childhood with easy bruising and bleeding, but had an otherwise unremarkable medical history. …”
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    Idiopathic splenomegaly in childhood and the spectrum of RAS-associated lymphoproliferative disease: a case report
  17. 31877
    “…CASE PRESENTATION: A 10.3-year-old Persian girl was brought to our clinic by her parents, with the complaint of failure to thrive and short height. …”
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    The value of a simple method to decrease diagnostic errors in Turner syndrome: a case report
  18. 31878
    “…While most transplanted patients achieved sustained SJIA remission off-treatment, the procedure-related morbidity was high. CASE REPORT: A girl presented SJIA with a severe disease course since the age of 15 months. …”
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    Sustained remission after haploidentical bone marrow transplantation in a child with refractory systemic juvenile idiopathic arthritis
  19. 31879
    “…CASE PRESENTATION: A 14-year-old Indian girl diagnosed with acute promyelocytic leukaemia currently undergoing a chemotherapy regimen that included all-trans retinoic acid/arsenic trioxide was sent to the radiology department for investigation of respiratory distress which she had developed soon after the initiation of chemotherapy. …”
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    Multidisciplinary corroboration in differentiation syndrome: a case report
  20. 31880
    “…A 25-year-old male patient, partly previously reported, was remarkable for childhood developed type 1 diabetes (T1D), transient growth hormone deficiency, and delayed puberty. The second case is a girl with an unusual presentation with central hypothyroidism and normal pigmentation of skin and hair. …”
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    Two Cases With an Early Presented Proopiomelanocortin Deficiency—A Long-Term Follow-Up and Systematic Literature Review
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