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Living with Intellectual disability-obesity-prognathism-eye and skin anomalies syndrome

A rare genetic syndrome with intellectual disability, obesity, a large lower jaw, and eye and skin differences.

Understanding Intellectual disability-obesity-prognathism-eye and skin anomalies syndrome

Intellectual disability-obesity-prognathism-eye and skin anomalies syndrome is a rare genetic syndrome with mild to profound intellectual disability and delayed speech.

Other features include obesity, eye differences such as droopy eyelids, crossed eyes, and lower visual sharpness, and long-lasting atopic dermatitis (eczema). Facial and jaw differences include a large head, a large lower jaw, and crowded teeth. It is present from birth.

Signs & symptoms

Symptoms vary from person to person. GARD lists these among the most common:

  • Intellectual disability and delayed speech
  • Obesity
  • Atopic dermatitis (eczema)
  • Eye muscle weakness (abducens palsy)
  • Large lower jaw
  • Crowded upper front teeth

Not everyone has every symptom. GARD's list comes from the Human Phenotype Ontology.

Diagnosis

  1. Talk with your doctor

    Share the symptoms you've noticed, when they started and your family health history. Notes and photos can help.

  2. See a specialist

    Specialists who may be involved include brain and nervous system specialists, genetic specialists and hormone specialists.

  3. Ask 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); Hormone specialists (endocrinologists)
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
Bring these questions to your next doctor visit
Can genetic testing help find the cause?
How can we manage eczema and eye problems?
Which specialists should care for the teeth and jaw?

Quick facts

Symptoms usually startNewborn
InheritanceAutosomal Recessive

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.

GeneticNeurologicalEndocrine

Also known as: intellectual disability, obesity, prognathism, eye and skin anomalies syndrome; momes syndrome

Patient organizations

Rare-disease groups that can help

Source: NIH GARD · Intellectual disability-obesity-prognathism-eye and skin anomalies syndromeGARD ID 17648 · GARD page updated September 2026 · Plain-language summary by Know Rare; editorial review pending. General information, not medical advice.

You are more than your diagnosis

Perspectives from people navigating life with Intellectual disability-obesity-prognathism-eye and skin anomalies syndrome.

Explore the Intellectual disability-obesity-prognathism-eye and skin anomalies syndrome blog

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