Browsing by Author "Radovich F."
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Alagille Syndrome: A review
Callea M.; Bahsi E.; Montanari M.; Ince B.; Mancini G.E.; Yavuz Y.; Radovich F. (2013)Alagille Syndrome (AGS) is a genetically determined multisystem disorder affecting liver, hearth, eyes, skeleton and facies, less commonly kidney and CNS. The prognosis depends on the severity of the associated anomalies. ... -
Bifid uvula and submucous cleft palate in cornelia de lange syndrome
Callea M.; Montanari M.; Radovich F.; Clarich G.; Yavuz I. (2011)Cornelia de Lange syndrome is a rare congenital disease characterized by growth and psychomotor retardation, peculiar facial feature as skeletal and craniofacial deformities, gastrointestinal and cardiac problems and ... -
Dental phenotype in a patient with hypoidrotic ectodermal dysplasia and severe immunodeficiency
Ectodermal dysplasia is a rare disease which affects at least two ectoderm-derived structures such as hair, nails, skin, sweat glands and teeth. The dentition is altered in number and shape. A 14-year-old male patient with ...