The 20 Best Culler Jones Syndrome Doctors Near Me in dubuque, IA

Find the Top Culler Jones Syndrome Experts and Specialists

Last Updated: 09/26/2026

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MediFind found 1 doctor with experience in Culler Jones Syndrome near dubuque, IA. Of these, 1 are Experienced.

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1 provider found
    Experienced in Culler Jones Syndrome

    Dr. Chadwick J. Nachtman
    Family Medicine
    Experienced in Culler Jones Syndrome

    Dr. Chadwick J. Nachtman
    Family Medicine
    Before you request

    Medical Associates Clinic - E.

    1000 Langworthy St., 
    Dubuque, IA 
     (1.0 miles away)
    563-584-3425
    Languages Spoken:
    English
    See accepted insurances
    Accepting New Patients

    Chadwick Nachtman is a primary care provider, practicing in Family Medicine in Dubuque, Iowa. Dr. Nachtman is rated as an Experienced provider by MediFind in the treatment of Culler Jones Syndrome. He is also highly rated in 36 other conditions, according to our data. His clinical expertise encompasses Familial Combined Hyperlipidemia, Xanthoma, Cirrhosis, and High Cholesterol. Dr. Nachtman is board certified in Family Medicine, American Board Of Family Medicine. Dr. Nachtman is currently accepting new patients.

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    Last Updated: 09/26/2026

    What is the definition of Culler Jones Syndrome?

    Culler-Jones syndrome is a rare disease characterized by pituitary anomalies resulting in hypopituitarism, presence of extra fingers (polydactyly) and unusual facial features. Symptoms related to the hypopituitarism may include abdominal pain, decreased appetite, short stature, delayed bone age, diabetes insipidus, slowed growth and sexual development, undescended testis (cryptorchidism) and small penis (hypogonadotropic hypogonadism). Facial features include eyes that appear very close together (hypotelorism), cleft palate and cleft lip and a flat nose. The extra digits are usually located on the outside of the little fingers (post-axial polydactyly). Brain imaging may show a small anterior pituitary gland. Culler-Jones syndrome is caused by changes in the GLI2 gene. Inheritance is autosomal dominant. Genetic changes in the GLI2 gene can also cause a different condition known as holoprosencephaly-9 (HPE9) which is much more severe. That condition is characterized by a single-lobed brain structure and severe skull and facial defects.