The 20 Best Albright's Hereditary Osteodystrophy Doctors Near Me in tallahassee, FL

Find the Top Albright's Hereditary Osteodystrophy Experts and Specialists

Last Updated: 09/26/2026

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MediFind found 1 doctor with experience in Albright's Hereditary Osteodystrophy near tallahassee, FL. Of these, 1 are Experienced.

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1 provider found
    Experienced in Albright's Hereditary Osteodystrophy

    Dr. Larry C. Deeb
    Pediatric Endocrinology
    Experienced in Albright's Hereditary Osteodystrophy

    Dr. Larry C. Deeb
    Pediatric Endocrinology
    Referral may be required

    Tmh Physician Partners-Endocrinology, Obesity & Diabetes

    2633 Centennial Blvd Ste 100, 
    Tallahassee, FL 
     (4.2 miles away)
    850-431-5404
    Languages Spoken:
    English
    See accepted insurances
    Accepting New Patients
    Offers Telehealth

    Larry Deeb is a Pediatric Endocrinologist practicing medicine in Tallahassee, Florida. Dr. Deeb is rated as an Experienced provider by MediFind in the treatment of Albright's Hereditary Osteodystrophy. He is also highly rated in 8 other conditions, according to our data. His clinical expertise encompasses Type 1 Diabetes (T1D), Pediatric Growth Hormone Deficiency, Growth Hormone Deficiency (GHD), and Panhypopituitarism. Dr. Deeb is currently accepting new patients.

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    Last Updated: 09/26/2026

    What is the definition of Albright's Hereditary Osteodystrophy?

    Albright's hereditary osteodystrophy (AHO) is a rare disorder with a wide range of signs and symptoms, including short stature, obesity, round face, subcutaneous ossifications (formation of bone under the skin), and short fingers and toes (brachydactyly). When the disorder is inherited from the mother, the features of AHO can be associated with resistance to certain hormones, in particular the parathyroid hormone (PTH). This is called pseudohypoparathyroidism type 1a (PHP1a). When inherited from the father, an individual will have AHO without any hormone issues, which is called pseudopseudohypoparathyroidism (PPHP). This condition is inherited in an autosomal dominant manner due to a genetic change in the GNAS gene.