Pseudopseudohypoparathyroidism, Albright Hereditary Osteodystrophy, autosomal dominant, brachymefaphalangia, brachydactily

Journal Title: Turkish Journal of Endocrinology and Metabolism - Year 1997, Vol 1, Issue 1

Abstract

Two cases of pseudopseudohypoparathyroidism with normal development and mental level, thyroid hyperplasia and without round faces are reviewed.

Authors and Affiliations

Figen Oksel, Nureddin Vurgun, Z. Ünlü, S. Tarhan, Esin Erkin, H. Ünlü, M. Solak, Ali Onağ, Baha Taneli

Keywords

Related Articles

The Relationship Between Glycosylated Haemoglobin and Diabetic Retinopathy in Patients with Type 2 Diabetes

Diabetes mellitus (DM) is a major health problem with long-term micro and macrovascular complications. Diabetic retinopathy (DR) is a sight-threating chronic complication of diabetes mellitus in adults. In this study, we...

Hashimoto's Encephalopathy

Hashimoto's Encephalopathy (HE) is a rare condition associated with Hashimoto's disease. HE is seen mostly in women. Researchers considered HE to consist of two sub types. HE is diagnosed in patients with neurological fi...

Papillary Carcinoma Incidentally Found in Graves’ Disease: A Case Report

Graves' disease is a benign disease and may be treated with anti-thyroid drugs, surgery or radioactive iodine. Patients with Graves' disease who have thyroid nodules should be evaluated more carefully due to the high ris...

Use of Metformin in Pregnancy: A Survey of Turkish Physicians’ Attitudes

Objective: Although metformin crosses the placenta, there is no current evidence whether the use of metformin in pregnancy is associated with increased risk of fetal and maternal complications. The aim of this present st...

The Levels of Serum High Sensitivity C-reactive Protein in Subjects with Impaired Fasting Glucose

High-sensitivity C-reactive protein is a well-known risk factor for cardiovascular heart diseases. In this study we aimed to determine the levels of serum high-sensitivity Creactive protein in patients with newly diagnos...

Download PDF file
  • EP ID EP83195
  • DOI -
  • Views 155
  • Downloads 0

How To Cite

Figen Oksel, Nureddin Vurgun, Z. Ünlü, S. Tarhan, Esin Erkin, H. Ünlü, M. Solak, Ali Onağ, Baha Taneli (1997). Pseudopseudohypoparathyroidism, Albright Hereditary Osteodystrophy, autosomal dominant, brachymefaphalangia, brachydactily. Turkish Journal of Endocrinology and Metabolism, 1(1), 45-48. https://europub.co.uk./articles/-A-83195