Psychiatry and Clinical Psychopharmacology

ALBRIGHT’S HEREDITARY OSTEODYSTROPHY AND DEMENTIA: A CASE REPORT

1.

Department of Psychiotry and Erciyes University School of Medicine

2.

Erciyes University School of Medicine, Department of Medical Genetics

3.

Erciyes University School of Medicine, Department of Endocrinology

4.

Erciyes University School of Medicine, Department of Neurology

5.

Erciyes Üniversitesi Tıp Fakültesi Psikiyatri AD, Kayseri, Türkiye

Psychiatry and Clinical Psychopharmacology 2001; 11: 183-186
Read: 791 Downloads: 534 Published: 10 March 2021

Albright’s Hereditary Osteodystrophy (AHO) is characterised by obesity, short stature, round face, brachydactyly, subcutaneous ossifications, mental retardation in some cases, hypocalcemia, and elevated serum parathyroid hormone (PTH) level. In this syndrome, there may be pseudohypoparathyroidism (PHP) characterised by end-organ unresponsiveness to PTH. In this report, we present an AHO case with unusual manifestation by presenting dementia which has not been previously reported.


Albright's Hereditary Osteodystrophy ve demans: Olgu sunumu

Albright'ın herditer osteodistrofisi (AHO) obezite, boy kısalığı, yuvarlak yüz, parmaklarda kısalık, cilt altı ossifikasyonlar, bazen mental retardasyon, hipokalsemi ve artmış serum paratiroid hormon (PTH) düzeyleri ile giden bir sendromdur. Bu sendromda PTH'a son organ cevapsızlığı ile karakterize olan yalancı hipoparatiroidizm (PHP) bulunabilir. Bu yazıda demans semptomları ile ortaya çıkan bir AHO olgusu sunulmuştur.

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EISSN 2475-0581