A novel variant in the GNAS complex locus causes Albright hereditary osteodystrophy with pseudopseudohypoparathyroidism

• Jeffrey S. Smith, MD, PhD,
• Abdulrahman A. Aldeeri, MD,
• Scott A. Elman, MD,
• Joel B. Krier, MD,
• Joseph F. Merola, MD, MMSc

Affiliations

Jeffrey S. Smith, MD, PhD

Department of Dermatology, Brigham and Women’s Hospital, Boston, Massachusetts; Department of Dermatology, Massachusetts General Hospital, Boston, Massachusetts; Department of Dermatology, Beth Israel Deaconess Medical Center, Boston, Massachusetts; Dermatology Program, Boston Children’s Hospital, Boston, Massachusetts; Harvard Medical School, Boston, Massachusetts

Abdulrahman A. Aldeeri, MD

Department of Dermatology, Brigham and Women’s Hospital, Boston, Massachusetts; Harvard Medical School, Boston, Massachusetts; Department of Genetics, Brigham and Women’s Hospital, Boston, Massachusetts; Division of Genetics and Genomics, Boston Children’s Hospital, Boston, Massachusetts; Department of Internal Medicine, King Saud University Medical City, Riyadh, Saudi Arabia

Scott A. Elman, MD

Department of Dermatology, Brigham and Women’s Hospital, Boston, Massachusetts; Department of Dermatology, Massachusetts General Hospital, Boston, Massachusetts; Department of Dermatology, Beth Israel Deaconess Medical Center, Boston, Massachusetts; Dermatology Program, Boston Children’s Hospital, Boston, Massachusetts; Harvard Medical School, Boston, Massachusetts

Joel B. Krier, MD

Department of Dermatology, Brigham and Women’s Hospital, Boston, Massachusetts; Department of Genetics, Brigham and Women’s Hospital, Boston, Massachusetts; Correspondence to: Joel B. Krier, MD, Division of Genetics, Department of Medicine, Brigham and Women's Hospital, Boston, MA.

Joseph F. Merola, MD, MMSc

Department of Dermatology, Brigham and Women’s Hospital, Boston, Massachusetts; Harvard Medical School, Boston, Massachusetts; Joseph F. Merola, MD, MMSc, Brigham and Women’s Hospital, 41 Avenue Louis Pasteur, Room 319, Boston, MA 02115.