Living with Epiphyseal dysplasia-hearing loss-dysmorphism syndrome
A very rare genetic condition with delayed development, hearing loss, short stature, and bone and facial differences.
Understanding Epiphyseal dysplasia-hearing loss-dysmorphism syndrome
It is seen in newborns. GARD also describes short stature, behavior challenges, patches of lighter skin, and differences in the thumbs and fingers. GARD notes no further reports in the medical literature since 1992.
Signs & symptoms
Symptoms vary from person to person. GARD lists these among the most common:
- Intellectual disability
- Delayed bone maturation
- Hearing loss from the inner ear
- Curved spine (scoliosis)
- Thumbs set close to the wrist
- Patches of lighter skin
Not everyone has every symptom. GARD's list comes from the Human Phenotype Ontology.
Diagnosis
- 1Talk with your doctor
Share the symptoms you've noticed, when they started and your family health history. Notes and photos can help.
- 2See a specialist
Specialists who may be involved include brain and nervous system specialists and genetic specialists.
- 3Ask which tests can help
Your care team will decide which exams and tests can confirm the diagnosis.
Care & treatment
- Care team
- Brain and nervous system specialists (neurologists); Genetic specialists (geneticists)
- Expert care
- Ask about multidisciplinary care centers for rare conditions
- Treatment
- GARD doesn't list specific treatments for this condition. Your care team will tailor care to your symptoms.
- Research
- Clinical trials and observational studies may be options. See the research section below.
General information, not medical advice. Your care team makes the decisions.
Everyday life
Living with a rare condition is easier with support.
- Connect with rare disease patient organizations for support
- Keep notes on symptoms, changes and questions for appointments
- Ask about patient registries that help research
- Look into financial aid and travel resources for care visits
Quick facts
Changes in genes cause this condition. GARD does not name the gene or how it is inherited.
Also known as: epiphyseal dysplasia-deafness-dysmorphism syndrome; epiphyseal dysplasia, hearing loss, dysmorphism syndrome; finucane kurtz scott syndrome; finucane-kurtz-scott syndrome
Patient organizations
Rare-disease groups that can help
- Global GenesRare Diseases · United States
- National Organization for Rare DisordersRare Diseases · United States
- Genetic AllianceRare Diseases · United States
- RARE FoundationRare Diseases · United States
You are more than your diagnosis
Perspectives from people navigating life with Epiphyseal dysplasia-hearing loss-dysmorphism syndrome.
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