Congenital disorders

Fetal congenital midaortic syndrome with unilateral renal artery stenosis prenatally presenting with polyhydramnios and postpartum as hyponatremic hypertensive syndrome
Sara Ardabili, Vincent Uerlings, Andrea Kaelin Agten, Markus Hodel

BMJ Case Reports CP May 2020, 13 (5) e234459; DOI: 10.1136/bcr-2020-234459
Duplication of the oral cavity and mandible: a rare congenital craniofacial anomaly
Alexandra O Hamberis, David Macias, Clarice Clemmens, Krishna G Patel

BMJ Case Reports CP May 2020, 13 (5) e233799; DOI: 10.1136/bcr-2019-233799
Postintravenous immunoglobulin stroke in a toddler with Down syndrome: a diagnostic challenge
Teck-Hock Toh, Everlyn Coxin Siew, Chae-Hee Chieng, Hussain Imam Mohd Ismail

BMJ Case Reports CP May 2020, 13 (5) e233149; DOI: 10.1136/bcr-2019-233149
Tetralogy of Fallot with absent pulmonary valve: main differences with classic Fallot are crucial for an accurate prenatal diagnosis and counselling
Rita Ataíde Silva, Duarte Martins, Ana Teixeira, Rui Anjos

BMJ Case Reports CP Apr 2020, 13 (4) e233592; DOI: 10.1136/bcr-2019-233592
Correction of a vertex encephalocele related to amniotic band syndrome
Aaron M Yengo-Kahn, Andreas C Plackis, Christopher M Bonfield, Srijaya K Reddy

BMJ Case Reports CP Mar 2020, 13 (3) e234735; DOI: 10.1136/bcr-2020-234735
Symptomatic scalp fistula present in a 14-month-old toddler
Jacob Gramacy, Sarah Sanford, Narlin B Beaty, Lutheria Hollis

BMJ Case Reports CP Mar 2020, 13 (3) e232103; DOI: 10.1136/bcr-2019-232103
Inherited cause of in utero digital malformations
Catherine Gooch, Caitlin Wright, Katherine Nelson, Nathaniel Robin

BMJ Case Reports CP Mar 2020, 13 (3) e232020; DOI: 10.1136/bcr-2019-232020
Phenotype and variations associated with the deletion of the 1q44 cytoband and the pathogenic duplication in the 9q32q34.3 cytobands
Ana Gómez-Carpintero García, Ana Vidal Esteban, Amanda Bermejo Gómez, Ruth Camila Púa Torrejón

BMJ Case Reports CP Mar 2020, 13 (3) e231938; DOI: 10.1136/bcr-2019-231938
Differentiating 11β-hydroxylase deficiency from primary glucocorticoid resistance syndrome in male precocity: real challenge in low-income countries
Sananda Majumder, Partha Pratim Chakraborty, Prakash Chandra Ghosh, Mitali Bera

BMJ Case Reports CP Feb 2020, 13 (2) e233722; DOI: 10.1136/bcr-2019-233722
Closing gastroschisis, vanishing midgut syndrome and intra-abdominal volvulus presenting with haematemesis at birth
Ahmed AbdElhamid Darwish

BMJ Case Reports CP Feb 2020, 13 (2) e232757; DOI: 10.1136/bcr-2019-232757

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Congenital disorders

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