💜 Parker’s Cure: Fueling Hope for HIST1H1E Syndrome

What Is HIST1H1E Syndrome?

HIST1H1E Syndrome — also known as H1-4 Syndrome or Rahman Syndrome — is a very rare genetic condition caused by a spontaneous change in a gene called HIST1H1E.
This gene makes a protein (linker histone H1.4) that helps package and regulate our DNA. When that process is disrupted, it affects how other genes turn on and off — influencing brain development, growth, skin, hair, teeth, hormones, and more.

Only about 50–65 children and adults have been identified worldwide, which means every family helps write the medical playbook as we go. Because the gene plays such a critical role in DNA structure, studying it can also unlock insights that stretch far beyond one diagnosis — into how our cells organize, repair, and regulate themselves.

Meet Parker 💜

Parker is a bright, loving, and determined 9-year-old who has faced extraordinary challenges since birth. From early developmental delays to ongoing medical hurdles affecting her growth, speech, and daily life, Parker’s journey has been anything but easy — yet her strength, laughter, and light continue to inspire everyone who knows her.

She has worked tirelessly through countless therapies and doctor visits, showing courage and resilience beyond her years. Parker’s smile, curiosity, and joy are what drive Parker’s Cure forward — reminding us every day why this fight matters so deeply.

What We’ve Learned So Far

Thanks to recent international studies and collaborations, doctors now recognize a more complete picture of the syndrome:

Developmental and intellectual delays of varying degrees are seen in nearly all patients.
Facial and ectodermal features — such as thin hair, fragile nails, and dental differences — are common.
Endocrine findings like thyroid issues and, in new 2024–2025 reports, short stature with pituitary hormone deficiencies have expanded what we know.
Bone and growth differences, heart findings, and behavioral features have been described in a growing number of cases.

Each new discovery brings us closer to understanding the underlying biology — and to identifying measurable targets for future therapies.

The Research: Dr. Yong-Hui Jiang and Yale School of Medicine

One of the world’s leading efforts is led by Dr. Yong-Hui Jiang, Chief of Medical Genetics at Yale School of Medicine.
His lab is using patient-derived stem cells, brain organoids, and mouse models to understand exactly how HIST1H1E mutations change gene expression and brain development.

In 2024, Dr. Jiang’s team received a major NIH grant and private philanthropic support — including gifts from Parker’s Cure families — to accelerate this work. They’re also collaborating with Couragene, Inc., a Yale-connected biotech developing gene-editing and gene-therapy platforms designed to eventually deliver corrective treatments for ultra-rare neurodevelopmental disorders like HIST1H1E Syndrome.

The goal is clear: move from understanding the mechanism to testing a targeted therapy — first in the lab, then in animal models, and ultimately in clinical trials.

The Impact of Parker’s Cure 💫

Since 2019, Parker’s Cure has been the driving force behind this progress — raising more than $775,000 through an incredible network of family, friends, and community supporters.
From our Bowling & Booze Bash 🎳 to our Color Run 🌈 and our new Let’s Glo Pickleball event 🎾, each dollar raised has directly supported the scientific work that brings us closer to a treatment.

We are so deeply grateful for the love and generosity of everyone who has rallied around this cause. What began as one family’s fight for Parker has become a nationwide effort to fuel groundbreaking research — proof that when a community shines together, miracles are possible.

Looking Ahead

Every milestone — each data point, each lab model, each new collaboration — moves us closer to what once felt impossible: a treatment, and someday a cure for Parker and every child with HIST1H1E Syndrome.

Your continued support makes that future real.
Together, we’re turning science into solutions, hope into healing, and light into life-changing progress. 💜✨

https://www.parkerscure.org/

https://medicine.yale.edu/news-article/large-nih-grant-supports-crispr-based-gene-therapy-development-for-brain-diseases/

https://hist1h1esyndrome.com/

Pickle for Parker- Let's Glo!

By HIST1H1E Genetic Syndrome Research Foundation Inc

Pickle for Parker- Let's Glo!