Disease: Acromegaloid hypertrichosis syndrome
- Acromegaloid facial appearance and hypertrichosis: a case suggesting autosomal recessive inheritance
- Acromegaloid facial appearance: case report and literature review
- An autosomal dominant syndrome of acromegaloid facial appearance and generalised hypertrichosis terminalis
- Approach to the Patient With Pseudoacromegaly
- Berardinelli-Seip congenital lipodystrophy in two siblings
- Cantu syndrome and hypopituitarism: implications for endocrine monitoring
- Cantu syndrome with coexisting familial pituitary adenoma
- Case Report: Loss-of-Function <em>ABCC9</em> Genetic Variant Associated With Ventricular Fibrillation
- De Novo Mutation in ABCC9 Causes Hypertrichosis Acromegaloid Facial Features Disorder
- Novel mutation in <em>ABBC9</em> gene associated with congenital hypertrichosis and acromegaloid facial features, without cardiac or skeletal anomalies: a new phenotype
- Novel mutation in ABBC9 gene associated with congenital hypertrichosis and acromegaloid facial features, without cardiac or skeletal anomalies: a new phenotype
- What's still unresolved in Hughes syndrome?
- Wide clinical variability in conditions with coarse facial features and hypertrichosis caused by mutations in ABCC9
- You "Cantu": Multidisciplinary Collaboration Resulting in Successful Orthognathic Surgery