Living with Intellectual disability-facial dysmorphism-hand anomalies syndrome
A rare syndrome with moderate intellectual disability, hand differences such as short or joined fingers, and distinct facial features.
Understanding Intellectual disability-facial dysmorphism-hand anomalies syndrome
Hand differences can include short fingers and joined fingers (syndactyly). Facial features include short eyelid openings, a bulbous nose tip, and a broad, pointed chin. Some people also have obesity, a small head, short stature, and a grimacing smile. It begins in the newborn period or infancy.
Signs & symptoms
Symptoms vary from person to person. GARD lists these among the most common:
- Moderate intellectual disability
- Delayed speech and language
- Learning disability
- Short eyelid openings
- Broad chin and broad nasal tip
- Short or joined fingers
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
GARD says it is inherited in an autosomal recessive pattern, meaning a child inherits a changed copy of the gene from each parent. It doesn't name a gene.
Also known as: intellectual disability, facial dysmorphism, hand anomalies 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 Intellectual disability-facial dysmorphism-hand anomalies syndrome.
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