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Developmental venous anomaly coexisting with arteriovenous malformation: a case report
Frontiers in SurgeryWe describe a rare case of a developmental venous anomaly associated with an arteriovenous malformation. A 20-year-old male presented with seizures and was diagnosed with left parietal arteriovenous malformation combined with developmental venous anomaly
Mei Li +6 more
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Radiology Case Reports, 2020 Hydrocephalus is a pathological buildup of cerebrospinal fluid within the ventricles leading to ventricular enlargement out of proportion to sulci and subarachnoid spaces.
Zhaoying Xian, MD +2 more
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Fetus in fetu – a rare developmental anomaly [PDF]
Radiology Case Reports, 2019 Fetus in fetu is a rare condition which most often presents as a fetiform calcified mass in the abdomen of its host, fetus or newborn. We report a case of 8-month-old girl with history of abdominal distension. Ultrasonography and computed tomography scan
Della Harigovind +3 more
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A Rare Case Report of Hypoplasia of Liver Lobe with Ectopia of Gall Bladder- Is Small Liver Lobe Always Pathological? [PDF]
International Journal of Anatomy Radiology and Surgery, 2021 Hypoplasia of right lobe of the liver with secondary ectopia of gall bladder is one of the rare morphological developmental anomalies of liver. Frequently, it is also associated with other hepatobiliary anomalies.
KANIMOZHI PERIASAMY, ANU EAPEN
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Regional odontodysplasia – a rare developmental dental anomaly
Pediatria Polska, 2021 Regional odontodysplasia is a rare developmental dental anomaly affecting ectodermal and mesodermal tissues. Hypocalcification and hypoplasia are most often observed in one quadrant.
Kacper Nijakowski, Anna Surdacka
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Esthetic-based Dental Management of Dentinogenesis Imperfecta in a 2.5-year-old Child [PDF]
Journal of Kerman University of Medical Sciences, 2021 Background: Dentinogenesis imperfecta (DI) is an autosomal dominant (AD) hereditary dentin disorder, which occurs in the absence of any systemic disorder. The patients with DI presented rapid and severe attrition in primary teeth, which causes functional
Leyli Sadri +3 more
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A Rare Co-occurrence of Amelogenesis Imperfecta (AI) and Various Non-Enamel Manifestations In Siblings-Report of Two Cases [PDF]
Journal of Clinical and Diagnostic Research, 2014 Amelogenesis Imperfecta (AI) is a hereditary enamel defect which is characterized by developmental abnormalities in the quantity and/ or quality of enamel.
A.J. Sai Sankar +3 more
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Journal of Indian Society of Pedodontics and Preventive Dentistry, 2011 Regional odontodysplasia is an unusual developmental anomaly in which ectodermal and mesodermal tooth components are affected. We present a rare case of a developmental anomaly called regional odontodysplasia or ′ghost teeth′ in a 12-year-old Indian girl.
D N Mehta, D Bailoor, B Patel
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Interdisciplinary Neurosurgery, 2018 A 21-year-old woman was admitted with a 1-day history of headache. Her neurological examination findings were normal. Computed tomography angiography revealed an oval, well-enhanced dilated vascular lesion in the anterior interhemispheric fissure with a ...
Hae-Won Koo +6 more
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Bilateral Fusion of Primary Mandibular Lateral Incisors and Canines: A Case Report [PDF]
Journal of Clinical and Diagnostic Research, 2020 Fusion is known as a developmental anomaly described by the union of two neighbouring teeth. The worldwide prevalence of bilaterally fused teeth in the primary dentition is about 0.02% which is considered very rare.
Sahar Fahad AlOtaibi +3 more
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