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Autor:
PrasannaKumar Rao, Anjali Ravi, HannahMaryam Mohiddin, BhargabiPaul Majumder, VishalS Nair, YR Girish, Deepak Pai, Raghavendra Kini, Nitin Gonsalves
Publikováno v:
Archives of Medicine and Health Sciences, Vol 9, Iss 2, Pp 302-305 (2021)
Gorlin-Goltz syndrome (GGS) is a hereditary condition; it is transmitted as an autosomal dominant trait and characterized by a wide range of developmental abnormalities and a tendency to neoplasm. This article includes a case report and an extensive