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Gorlin syndrome: A case report

Gorlin syndrome is a rare autosomal dominant disorder which characterize by multi-organ abnormities such as odontogenic keratocysts in the jaw, skeletal abnormities and multiple basal cell carcinoma etc. We report a case of this syndrome in a young man with palmar pits, multiple facial BCC, clacific...

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Príomhchruthaitheoirí:	Abbas Darjani (Údar), Hojat Eftekhari (Údar), Nahid Nickhah (Údar)
Formáid:	LEABHAR
Foilsithe / Cruthaithe:	Our Dermatology Online, 2016-01-01T00:00:00Z.
Ábhair:	article
Rochtain ar líne:	Connect to this object online.
Clibeanna:	Cuir clib leis Níl clibeanna ann, Bí ar an gcéad duine le clib a chur leis an taifead seo!

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