Surprising genetic and pathological findings in a patient with giant bilateral periadrenal tumours: PEComas and mutations of PTCH1 in Gorlin-Goltz syndrome.
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DOI: 10.1136/jmedgenet-2021-108082
Abstract: Gorlin-Goltz syndrome (GGS) or nevoid basal cell carcinoma syndrome is a rare tumour-overgrowth syndrome associated with multiple developmental anomalies and a wide variety of tumours. Here, we describe a case of a man aged 23… read more here.
Keywords: gorlin goltz; surprising genetic; goltz syndrome; tumours pecomas ... See more keywords