The 20 Best Griscelli Syndrome Doctors Near Me in middletown, DE

Find the Top Griscelli Syndrome Experts and Specialists

Last Updated: 09/26/2026

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MediFind found 2 doctor with experience in Griscelli Syndrome near middletown, DE. Of these, 1 are Advanced and 1 are Experienced.

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2 providers found
    Experienced in Griscelli Syndrome
    Experienced in Griscelli Syndrome
    Referral may be required

    Sunwise Dermatology & Surgery LLC

    102 Sleepy Hollow Dr Ste 203, 
    Middletown, DE 
     (3.8 miles away)
    Languages Spoken:
    English
    Accepting New Patients

    Jennifer Larusso is a Dermatologist practicing medicine in Middletown, Delaware. Dr. Larusso is rated as an Experienced provider by MediFind in the treatment of Griscelli Syndrome. She is also highly rated in 5 other conditions, according to our data. Her clinical expertise encompasses Liver Spots, Universal Acquired Melanosis, Bowen's Disease, and Keloids. Dr. Larusso is currently accepting new patients.

    Advanced in Griscelli Syndrome
    Pediatrics | Internal Medicine
    Advanced in Griscelli Syndrome
    Pediatrics | Internal Medicine
    Referral may be required

    Bear Internal Medicine And Pediatrics

    1400 Peoples Plaza, Suite 201, 
    Newark, DE 
     (10.7 miles away)
    Languages Spoken:
    English
    Accepting New Patients

    Shilpa Mehta is a primary care provider, practicing in Pediatrics and Internal Medicine in Newark, Delaware. Dr. Mehta is rated as an Advanced provider by MediFind in the treatment of Griscelli Syndrome. She is also highly rated in 4 other conditions, according to our data. Her clinical expertise encompasses Dyschromatosis Symmetrica Hereditaria, Dyschromatosis Universalis Hereditaria, Hypomelanotic Disorder, and Griscelli Syndrome. Dr. Mehta is currently accepting new patients.

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    Last Updated: 09/26/2026

    What is the definition of Griscelli Syndrome?

    Griscelli syndrome is an inherited condition characterized by unusually light (hypopigmented) skin and light silvery-gray hair starting in infancy. Researchers have identified three types of this disorder, which are distinguished by their genetic cause and pattern of signs and symptoms.

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