Wiedemann-Rautenstrauch syndrome

Wiedemann-Rautenstrauch syndrome is a very rare disorder with features of premature aging recognizable at birth, decreased subcutaneous fat, hypotrichosis, relative macrocephaly and dysmorphism.

Also known as: Wiedemann Rautenstrauch Syndrome, Wiedemann-Rautenstrauch syndrome, neonatal progeroid syndrome, Wiedemann Rautenstrauch syndrome, progeroid syndrome neonatal.

Category: General

Looking into Wiedemann-Rautenstrauch syndrome? See the lab tests healthcare providers may use to investigate Wiedemann-Rautenstrauch syndrome, and learn what each one measures.
Explore tests for Wiedemann-Rautenstrauch syndrome
Symptoms

Symptoms associated with Wiedemann-Rautenstrauch syndrome

The following symptoms have been associated with Wiedemann-Rautenstrauch syndrome in medical literature. Not everyone experiences the same symptoms.

Tests

Tests used to investigate Wiedemann-Rautenstrauch syndrome

Healthcare providers may order these tests when evaluating Wiedemann-Rautenstrauch syndrome. Test selection is a clinical decision made by a qualified professional.

CBC with Differential

Measures red blood cells, white blood cells, and platelets to help evaluate overall health and detect disorder...

Sample: Blood

Comprehensive Metabolic Panel (CMP)

Measures 14 substances in the blood to assess kidney and liver function, electrolyte balance, and blood sugar ...

Sample: Blood

Urinalysis

Examines urine content to help detect urinary tract infections, kidney disease, and diabetes....

Sample: Urine

Related conditions

Conditions with overlapping symptoms

These conditions share symptoms with Wiedemann-Rautenstrauch syndrome, which is why a clinical evaluation is important.

FAQ

Frequently Asked Questions

What is Wiedemann-Rautenstrauch syndrome?

Wiedemann-Rautenstrauch syndrome is a health condition described in medical literature. Wiedemann-Rautenstrauch syndrome is a very rare disorder with features of premature aging recognizable at birth, decreased subcutaneous fat, hypotrichosis, relative macrocephaly and dysmorphism.

What are the symptoms of Wiedemann-Rautenstrauch syndrome?

Wiedemann-Rautenstrauch syndrome is associated with 8 symptoms in the medical literature we index, including Alopecia, Alopecia of scalp, Deeply set eye, Dry skin, Dysphagia, Failure to thrive. Symptoms vary widely between individuals.

How is Wiedemann-Rautenstrauch syndrome diagnosed or investigated?

A healthcare provider may use a combination of medical history, physical examination, and tests. Common tests associated with Wiedemann-Rautenstrauch syndrome include CBC with Differential, Comprehensive Metabolic Panel (CMP), Urinalysis. This information is educational, not a diagnosis.

Is SymptomDatabase.com diagnosing me?

No. SymptomDatabase.com does not provide diagnosis. If you are concerned you may have Wiedemann-Rautenstrauch syndrome, please discuss your symptoms with a qualified healthcare provider.

Educational content only: The information on Symptom Database.com is for educational purposes and is not medical advice, diagnosis, or treatment. Always consult a qualified healthcare provider. Read our full disclaimer.