The 20 Best Hereditary Mucoepithelial Dysplasia Doctors Near Me in petersburg, IN

Find the Top Hereditary Mucoepithelial Dysplasia Experts and Specialists

Last Updated: 09/26/2026

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MediFind found 1 doctor with experience in Hereditary Mucoepithelial Dysplasia near petersburg, IN. Of these, 1 are Experienced.

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1 provider found
    Experienced in Hereditary Mucoepithelial Dysplasia
    Family Medicine
    Experienced in Hereditary Mucoepithelial Dysplasia
    Family Medicine

    Dycora Transitional Health-Petersburg LLC

    309 W Pike Ave, 
    Petersburg, IN 
     (0.9 miles away)
    Languages Spoken:
    English
    Accepting New Patients

    Nathanial Grow is a primary care provider, practicing in Family Medicine in Petersburg, Indiana. Dr. Grow is rated as an Experienced provider by MediFind in the treatment of Hereditary Mucoepithelial Dysplasia. He is also highly rated in 13 other conditions, according to our data. His clinical expertise encompasses High Cholesterol, Glucocorticoid-Remediable Aldosteronism, Hypertension, and Familial Hypertension. Dr. Grow is currently accepting new patients.

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    Last Updated: 09/26/2026

    What is the definition of Hereditary Mucoepithelial Dysplasia?

    Hereditary mucoepithelial dysplasia (HMD) is a condition that affects the skin, hair, mucosa (areas of the body that are lined with mucus), gums (gingiva), eyes, nose and lungs. Symptoms begin in infancy and vary in severity from person to person. The most common symptoms of this condition include hair loss (alopecia), patchy red skin around the perineum (the area between the anus and external genitalia); and red gums. Small, skin-colored bumps (keratosis pilaris) and early development of cloudy lens (cataracts) are also common. Other symptoms may include eye disease that gets worse over time, lung disease and a rough, red tongue. Intelligence is normal. The exact cause of HMD is still unknown, but it is thought to be an abnormality in desmosomes and gap junctions, which are cell structures involved in cell-to-cell contact. HMD appears to be inherited in an autosomal dominant pattern, but has occurred in individuals with no family history of the condition. The diagnosis of HMD is based on the symptoms and other skin and eye disorders need to be excluded.

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