Simpson–Golabi–Behmel syndrome in a 39‐year‐old male patient with suspected acromegaly

Simpson–Golabi–Behmel syndrome in a 39‐year‐old male patient with suspected acromegaly—A case study

Published:2018-12-28 Issue:2 Volume:179 Page:322-328
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am J Med Genet Part A

Author:

Andrysiak‐Mamos Elżbieta¹,Sagan Karol Piotr¹^ORCID,Lietz‐Kijak Danuta²,Kijak Edward³,Kaźmierczak Beata⁴,Pietrzyk Aleksandra⁵,Sowinska‐Przepiera Elżbieta¹,Sagan Leszek⁶,Syrenicz Anhelli¹

Affiliation:

1. Pomeranian Medical UniversityDepartment of Endocrinology, Metabolic and Internal Diseases Szczecin Poland

2. Pomeranian Medical University, Independent Unit of Propaedeutic and Dental Physical DiagnosticsFaculty of Medicine and Dentistry Szczecin Poland

3. Pomeranian Medical UniversityScientific Unit of Dysfunction of the Masticatory System, Faculty of Medicine and Dentistry, Department of Prosthodontics Szczecin Poland

4. Pomeranian Medical UniversityOphthalmology Clinic Szczecin Poland

5. Pomeranian Medical UniversityGenetic Outpatient Clinic Szczecin Poland

6. Pomeranian Medical UniversityDepartment of Neurosurgery and Pediatric Neurosurgery Szczecin Poland

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.61013

Reference22 articles.

1. A new X-linked dysplasia gigantism syndrome: Identical with the Simpson dysplasia syndrome?

2. Glypican-3 binds to frizzled and plays a direct role in the stimulation of canonical Wnt signaling