Acrorenal mandibular syndrome
| Acrorenal mandibular syndrome | |
|---|---|
| Synonyms | Acrorenal syndrome, Acrorenal mandibular dysplasia |
| Pronounce | N/A |
| Specialty | N/A |
| Symptoms | Limb abnormalities, renal anomalies, mandibular hypoplasia |
| Complications | Kidney failure, respiratory difficulties |
| Onset | Congenital |
| Duration | Lifelong |
| Types | N/A |
| Causes | Genetic mutation |
| Risks | Family history |
| Diagnosis | Clinical examination, genetic testing |
| Differential diagnosis | Branchio-oto-renal syndrome, Nager syndrome |
| Prevention | N/A |
| Treatment | Supportive care, surgical intervention |
| Medication | N/A |
| Prognosis | Variable |
| Frequency | Rare |
| Deaths | N/A |
Alternate names
ACRPS; Syndactyly, preaxial polydactyly and sternal deformity; ACRP syndrome; Acro-pectoral syndrome
Definition
A rare syndrome characterized by a combination of distal limb abnormalities (syndactyly of all fingers and toes, preaxial polydactyly in the feet and/or hands) and upper sternum malformations.
NIH genetic and rare disease info
Acrorenal mandibular syndrome is a rare disease.
| Rare and genetic diseases | ||||||
|---|---|---|---|---|---|---|
|
Rare diseases - Acrorenal mandibular syndrome
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Resources
| Additional resources | ||
|---|---|---|
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Acrorenal mandibular syndrome
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