Disease: Acromegaloid facial appearance syndrome
- A new case of acromegaloid facial appearance (AFA) syndrome with an expanded phenotype
- A new case of the acromegaloid facial appearance syndrome?
- Acromegaloid facial appearance (AFA) syndrome: report of a second family
- Acromegaloid facial appearance and hypertrichosis: a case suggesting autosomal recessive inheritance
- Acromegaloid facial appearance syndrome
- Acromegaloid facial appearance syndrome: a further case report
- Acromegaloid facial appearance: case report and literature review
- Acromegaly with congenital generalized lipodystrophy - two rare insulin resistance conditions in one patient: a case report
- An autosomal dominant syndrome of acromegaloid facial appearance and generalised hypertrichosis terminalis
- An autosomal dominant syndrome with 'acromegaloid' features and thickened oral mucosa
- Cantu syndrome and hypopituitarism: implications for endocrine monitoring
- Cantú syndrome with coexisting familial pituitary adenoma
- Case Report: Loss-of-Function <em>ABCC9</em> Genetic Variant Associated With Ventricular Fibrillation
- Cloning, mapping, and expression analysis of TBX15, a new member of the T-Box gene family
- De Novo Mutation in ABCC9 Causes Hypertrichosis Acromegaloid Facial Features Disorder
- Looking for the skeleton in the closet-rare genetic diagnoses in patients with diabetes and skeletal manifestations
- Novel mutation in <em>ABBC9</em> gene associated with congenital hypertrichosis and acromegaloid facial features, without cardiac or skeletal anomalies: a new phenotype
- Pachydermoperiostosis: a rare mimicker of acromegaly
- What you need to know about migraine in Hughes syndrome patients
- What's still unresolved in Hughes syndrome?
- Wide clinical variability in conditions with coarse facial features and hypertrichosis caused by mutations in ABCC9