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RESEARCH STUDIES FOR MALAN SYNDROME

Study Title: Observational Study Evaluating Natural History, Clinical Progression, and Patient-Reported Outcomes in Malan Syndrome

Principal Investigator: Jennifer Kalish, MD, PhD

Research Institution: Children's Hospital of Philadelphia

Status: Enrolling

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This study aims to characterize the natural history and clinical progression of Malan syndrome by reviewing the signs and symptoms of the syndrome, including symptom severity, and functional outcomes in patients with genetically confirmed Malan syndrome. Specifically, this study will observe the effects of clinician-prescribed medications on symptom mitigation as well as behavior, sleep, and communication ability.

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Enroll here

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If you need additional information, please contact overgrowthresearch@chop.edu

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Study Title: Comprehensive Dental History Evaluation in Malan Syndrome

Principal Investigator: Benjamin Cocanougher, MD, PhD

Research Institution: Cincinnati Children's Hospital 

Status: Enrolling until March 31, 2026

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The purpose of this study is to better understand oral health, dental development, and craniofacial features in individuals with Malan syndrome.

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What Participation Involves
If you agree to take part, your participation will include completing a one-time survey about the dental history for yourself or the individual you care for.
This survey will include questions about:

  • Tooth development

  • Dental or oral health concerns

  • Dental care history

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Who Can Participate

  • Any individual with a diagnosis of Malan syndrome

  • All ages welcome

  • Parent/primary caregiver with English fluency

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Risks, Benefits, Costs, Payment
There are no known risks associated with participating in this study. There are no direct benefits to you personally; however, your participation may help improve our understanding of and future dental care for individuals with Malan syndrome.


Participation is entirely voluntary, and you may withdraw at any time. There is no cost to participate and you will not receive payment for completing the survey.

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Enroll and complete the survey here.

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If you need additional information, please contact the research coordinator for this study, Kaitlynn Jenkins, at 513-636-2811 or kaitlynn.stowers@cchc.org

DISCLAIMER

Le informazioni fornite su questo sito Web non intendono sostituire la consulenza medica professionale. Nessuna immagine su questo sito può essere utilizzata senza il consenso scritto della Fondazione Sindrome di Malan.

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