Rare Diseases Symptoms Automatic Extraction

Hypogonadotropic hypogonadism associated with hereditary hemorrhagic telangiectasia [corrected].

[kallmann syndrome]

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.

Diseases presenting "telangiectasia" symptom

  • coats disease
  • cowden syndrome
  • cutaneous mastocytosis
  • hereditary cerebral hemorrhage with amyloidosis
  • kallmann syndrome
  • kindler syndrome
  • malignant atrophic papulosis
  • omenn syndrome
  • pendred syndrome
  • severe combined immunodeficiency
  • systemic capillary leak syndrome
  • triple a syndrome
  • waldenström macroglobulinemia
  • werner syndrome

This symptom has already been validated