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Tag Archives: Diagnosis
Defining a fetal deprivation sequence
Intrauterine growth restriction (IUGR) as a consequence of substrate deficiency has many detrimental effects on the fetus. These effects clinically present with multi-organ dysfunction. Detailed investigation of potentially affected cases was conducted in conjunction with a literature review to enable … Continue reading
Diagnosis and care of the newborn with epidermolysis bullosa
Epidermolysis bullosa (EB) is a group of rare genetic disorders that are characterized by fragile skin. Because of its rarity, many neonatologists may not be familiar with the current diagnosis and treatment recommendations for EB. The classification of EB was … Continue reading
Posted in Uncategorized
Tagged Diagnosis, Epidermolysis Bullosa, Newborns, treatments
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Congenital epulis and differential diagnoses of a neonatal oral mass
Oral mass in a newborn is rare but often quite daunting, leading to anxiety in parents. Very few hospitals have dental or maxillofacial facilities on site and this may lead to delayed diagnosis and intervention. A thorough clinical examination and … Continue reading
Revisiting skeletal dysplasias in the newborn
With over 400 reported disorders, the skeletal dysplasias represent a myriad of molecularly-based skeletal abnormalities. Arising from errors in skeletal development, the clinical spectrum of disease evolves through an affected individual’s life. The naming and grouping of these disorders are … Continue reading
Perinatal stroke: a practical approach to diagnosis and management
Perinatal stroke is a focal vascular brain injury that occurs from the fetal period to 28 days of postnatal age. With an overall incidence of up to 1 in 1,000 live births, the most focused lifetime risk for stroke occurs … Continue reading
Posted in Uncategorized
Tagged Diagnosis, focal vascular brain injury, neonatal period, neonate, Perinatal stroke
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Neonatal care 