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Paediatrics
- Neurological Waardenburg-Shah syndrome: a diagnostic challenge in a child with skin hypopigmentation and neurological manifestationBenjamin Wei-Liang Ng, Jeffrey Soon-Yit Lee, Teck-Hock Toh, Lock-Hock NguBMJ Case Reports CP Jun 2022, 15 (6) e250360; DOI: 10.1136/bcr-2022-250360
- Prenatal diagnosis of fetal hemivertebra at 12 weeks of gestationDiana Monteiro, Inês Sarmento Gonçalves, Cristina Godinho, Rosete Novais NogueiraBMJ Case Reports CP Jun 2022, 15 (6) e251293; DOI: 10.1136/bcr-2022-251293
- Thoracic venous malformation: a particular form of a visceral variantInês Pessanha, Paloma Triana, Victor Martinez-Glez, Juan Carlos Lopez-GutierrezBMJ Case Reports CP Jun 2022, 15 (6) e250307; DOI: 10.1136/bcr-2022-250307
- Acute inhalation lung injury secondary to zinc and copper aspiration from food contact dustJames Moss, Aditi Sinha, Shrouk Messahel, Christopher GrimeBMJ Case Reports CP Jun 2022, 15 (6) e250152; DOI: 10.1136/bcr-2022-250152
- Inborn error of metabolism precipitated by COVID-19: challenges in the absence of an expanded newborn screening as state health programmesPriyanka Olety, Gundyadka Moideen Safwan, Rathika Damodara ShenoyBMJ Case Reports CP Jun 2022, 15 (6) e248001; DOI: 10.1136/bcr-2021-248001
- ‘Miliary metastasis’ in a child with papillary thyroid cancerAndre Gie, Pawel Schubert, Wilhelmina Conradie, Pierre GoussardBMJ Case Reports CP Jun 2022, 15 (6) e249598; DOI: 10.1136/bcr-2022-249598
- Atypical trigeminocardiac reflex during intranasal dexmedetomidine sedation of a 6-month-old premature babyDenise Bayard, Friedrich Lersch, Gesar Ugen, Bernhard SchallerBMJ Case Reports CP May 2022, 15 (5) e247292; DOI: 10.1136/bcr-2021-247292
- Filariasis presenting as pancytopenia in a childAnusree Krishna Mandal, Jadab Kumar Jana, Soumya Gayen, Abhay Charan PalBMJ Case Reports CP May 2022, 15 (5) e248930; DOI: 10.1136/bcr-2022-248930
- Zinner syndrome: a rare diagnosis in infancyJoanne Michelle Oida Rose, Ravi Banthia, Zain Tamboli, Hira LalBMJ Case Reports CP May 2022, 15 (5) e248558; DOI: 10.1136/bcr-2021-248558
- Rare paediatric case of agenesis of the vermiform appendix, ileal duplication and sickle cell diseaseNadia Laezza, Nuno Gião, Cristina Borges, Maria KnoblichBMJ Case Reports CP May 2022, 15 (5) e248181; DOI: 10.1136/bcr-2021-248181
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