Albright Hereditary Osteodystrophy: A Case Report
Published: October 1, 2014 | DOI: https://doi.org/10.7860/JCDR/2014/.5041
Deepa Hugar, Sangameshwar Sajjanshetty, Santosh Hugar, Megha Kadani
1. Senior Lecturer, Department of Oral and Maxillofacial Pathology, H.K.E.S’s S.Nijalingappa Institute of Dental Sciences & Research,
Sedam Road, Gulbarga, Karnataka, India.
2. Reader, Department of Pedodontics and Preventive Dentistry, H.K.E.S’s S.Nijalingappa Institute of Dental Sciences & Research,
Sedam Road, Gulbarga, Karnataka, India.
3. Reader, Department Conservative and Endodontics, Bharatiya Vidyapeeth Dental College and Hospital, Sangli, Maharastra, India.
4. Post Graduate, Department of Oral and Maxillofacial Pathology, H.K.E.S’s S.Nijalingappa Institute of Dental Sciences & Research,
Sedam Road, Gulbarga, Karnataka, India.
Correspondence
Dr. Deepa Hugar,
Senior Lecturer, Department of Oral Pathology,
H.K.E.S’s S.Nijalingappa Institute of Dental Sciences & Research, Sedam Road, Gulbarga-585103, India.
Phone : +91-9535145941, E-mail : drdeepahugar@gmail.com
A dental practitioner with an eagle’s eye can diagnose many hidden disease through careful examination of the oral cavity. One such hereditary metabolic disorder is Albright hereditary osteodystrophy (AHO). Characteristic presentations in an individual affected by AHO were short stature, obesity and brachydactyly especially of 4th and 5th digits, which are the phenotypic features of genetic mutation. Pseudohypoparathyroidism (PHP) is characterized by inability of the body to respond appropriately to parathormone, mainly characterized by hypocalcemia, increased serum parathormone concentration, insensitivity to the biological activity of parathormone and hyperphosphatemia. AHO when seen in association with resistance to parathormone (PTH), it is called PHP. Here is, a case report of 32-year-old male patient with AHO with distinctive physical characteristics and oral manifestations
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