Short answer · Medically reviewed summary · Last updated: 2026-05-08
Acromicric dysplasia is a rare form of skeletal dysplasia characterized by short stature, short hands and feet, and distinct facial features. While it is most commonly referred to by this name, it may occasionally appear in older clinical literature or international databases under synonyms such as acromicric skeletal dysplasia or as part of the spectrum of acromelic dysplasias. What are the official names and synonyms for Acromicric Dysplasia? In modern medical practice, Acromicric dysplasia is the standard terminology used by geneticists and clinicians.
Acromicric Dysplasia synonyms
Other names for Acromicric Dysplasia: synonyms, acronyms and related terms used by doctors and patients.
Acromicric dysplasia is a rare form of skeletal dysplasia characterized by short stature, short hands and feet, and distinct facial features. While it is most commonly referred to by this name, it may occasionally appear in older clinical literature or international databases under synonyms such as acromicric skeletal dysplasia or as part of the spectrum of acromelic dysplasias.
What are the official names and synonyms for Acromicric Dysplasia?
In modern medical practice, Acromicric dysplasia is the standard terminology used by geneticists and clinicians. However, patients may encounter various terms depending on the era of the publication or the classification system used. Historically, Acromicric dysplasia was sometimes categorized alongside other conditions affecting the distal limbs. It is officially listed in the Online Mendelian Inheritance in Man (OMIM) database under the entry #102370. In the Orphanet database, it is identified by the code ORPHA:1396.
Why does Acromicric Dysplasia have multiple names?
The nomenclature for Acromicric dysplasia reflects the evolution of clinical genetics. Before the identification of the FBN2 gene as the underlying cause, the condition was primarily described by its phenotypic characteristics, leading to descriptive terms. Because Acromicric dysplasia shares clinical features with geleophysic dysplasia—both being acromelic dysplasias caused by mutations in the FBN2 gene—medical literature sometimes groups them together, which can lead to confusion in older medical records.
How is the condition classified in medical systems?
- OMIM ID: #102370
- Orphanet ID: ORPHA:1396
- ICD-10/11: Often coded under "Other specified osteochondrodysplasias" due to its extreme rarity.
- Clinical classification: Member of the fibrillinopathy spectrum.
Currently, the medical community prefers Acromicric dysplasia because it specifically denotes the "small" (micric) nature of the "extremities" (acro), providing a precise clinical description that aligns with international diagnostic standards.
Next steps
- Consult a clinical geneticist to review your specific diagnostic report and ensure the correct terminology is used in your medical files.
- Connect with the DiseaseMaps.org community, where 3 individuals living with Acromicric dysplasia share their experiences and insights.
- Review your records for any older, outdated diagnostic labels to ensure your current care team is using the most accurate terminology.
Medical disclaimer: This information is for educational purposes only and should not replace professional medical advice, diagnosis, or treatment; always seek the advice of a qualified physician with any questions regarding a medical condition.
References
- Online Mendelian Inheritance in Man (OMIM): Entry #102370.
- Orphanet: Rare Disease Database (ORPHA:1396).
- NIH Genetic and Rare Diseases Information Center (GARD).
- PubMed: Latest clinical literature regarding FBN2-related skeletal dysplasias.
