The 20 Best Congenital Erythropoietic Porphyria Doctors Near Me in flowood, MS

Find the Top Congenital Erythropoietic Porphyria Experts and Specialists

Last Updated: 09/26/2026

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MediFind found 2 doctor with experience in Congenital Erythropoietic Porphyria near flowood, MS. Of these, 2 are Experienced.

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2 providers found
    Experienced in Congenital Erythropoietic Porphyria
    Experienced in Congenital Erythropoietic Porphyria
    Referral may be required
    Before you request

    University Pathology Associates PLLC

    2500 N State St, 
    Jackson, MS 
     (4.5 miles away)
    601-815-2005
    Languages Spoken:
    English
    See accepted insurances
    Accepting New Patients

    Jeremy Jackson is a Dermatologist practicing medicine in Jackson, Mississippi. Dr. Jackson is rated as an Experienced provider by MediFind in the treatment of Congenital Erythropoietic Porphyria. He is also highly rated in 10 other conditions, according to our data. His clinical expertise encompasses Lymphomatoid Papulosis, Cutaneous T-Cell Lymphoma (CTCL), Anaplastic Large Cell Lymphoma, and T-Cell Lymphoma. Dr. Jackson is currently accepting new patients.

    Experienced in Congenital Erythropoietic Porphyria
    Experienced in Congenital Erythropoietic Porphyria
    Referral may be required

    Children's Of Mississippi Hospital-Blair E. Batson Tower

    1010 Lakeland Pl, 
    Flowood, MS 
     (4.6 miles away)
    601-815-4506
    Languages Spoken:
    English
    See accepted insurances
    Offers Telehealth

    Robert Brodell is a Dermatologist practicing medicine in Flowood, Mississippi. Dr. Brodell is rated as an Experienced provider by MediFind in the treatment of Congenital Erythropoietic Porphyria. He is also highly rated in 15 other conditions, according to our data. His clinical expertise encompasses Basal Cell Skin Cancer, Squamous Cell Skin Carcinoma, Dermatitis Herpetiformis, and Punctate Porokeratosis.

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    Last Updated: 09/26/2026

    What is the definition of Congenital Erythropoietic Porphyria?

    Congenital erythropoietic porphyria (CEP) is the rarest type of porphyria and is commonly seen in infancy. It is characterized by severe skin photosensitivity that may lead to scarring, blistering, and increased hair growth at the face and back of the hands. Photosensitivity and infection may cause the loss of fingers and facial features. Symptoms of CEP range from mild to severe and may include excessive hair growth throughout the body (hypertrichosis), reddish discoloration of the teeth, anemia, and reddish-colored urine. In CEP, there is a defect in the synthesis of heme within the red blood cells of bone marrow. This defect leads to an increase in the buildup and, therefore, waste of porphyrin and its precursors, which leads to the signs and symptoms. Inheritance is autosomal recessive. It is caused by genetic changes in the UROS gene.