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Hypogonadotropic hypogonadism associated with hereditary hemorrhagic telangiectasia [corrected]. 2013
Valentina Scarano, and
Scarano Valentina, and
Daniele De Santis, and
De Santis Daniele, and
Patrizia Suppressa, and
Suppressa Patrizia, and
Patrizia Lastella, and
Lastella Patrizia, and
Gennaro Mariano Lenato, and
Lenato Gennaro Mariano, and
Vincenzo Triggiani, and
Triggiani Vincenzo, and
Carlo Sabbà, and
Sabbà Carlo
Neurology Unit, "S. Maria del Pozzo" Hospital, Somma Vesuviana, 80049 Naples, Italy.
A 65-year-old man was referred to our clinic for the rehabilitation of right hemiparesis caused by ischaemic stroke. Hypertension, postphlebitic syndrome of lower limbs, frequent nose bleeding, and anemia were present in his history; in his adolescence, he was treated for idiopathic hypogonadotropic hypogonadism. Further investigations have revealed also microsomia, suggesting a clinical diagnosis of Kallmann syndrome, that is, an association, possible in males and females, of hypogonadotropic hypogonadism with olfactory deficits. A definite diagnosis of hereditary hemorrhagic telangiectasia was made based on clinical criteria and confirmed by genetic analysis.
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