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| Disease found: | Baird syndrome - Absence of Fingerprints |
| Current as of: | Thu Nov 21 2024 |
| Disease Overview: | Poorly understood genetic syndrome (familial and sporadic) appears to be autosomal dominant affecting dermal formation and structure in infants and children [more info] |
| Signs and Symptoms: | Blisters and facial milia in early childhood, congenital absence of dermatoglyphics on the hands and feet, thin skin, camptodactyly, hypohidrosis [more info] |
| Diagnosis: | Clinical exam and genetic testing (WES) [more info] |
| Treatment: | Supportive Treatment Only [more info] |
| Clinical Management: | Support for ADLs due to increased skin fragility [more info] |
| Referral: | No specific physicians specialize in this condition, often managed by dermatology. Referral to Medical Genetics Department, if available. Initial virtual care is also available through organizations like TeleRare Health. |
| Clinical Trials: | None are available, but can sign up to be notified when one becomes available |