renal hypomagnesemia 3

Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement (FHHN) is a form of familial primary hypomagnesemia (FPH), characterized by recurrent urinary tract infections, nephrolithiasis, bilateral nephrocalcinosis, renal magnesium (Mg) wasting, hypercalciuria and kidney failure.

Also known as: CLDN16 familial primary hypomagnesemia, CLDN16 primary hypomagnesemia, FHHNC without severe ocular involvement, HOMG3, familial primary hypomagnesemia caused by mutation in CLDN16, primary hypomagnesemia caused by mutation in CLDN16, renal hypomagnesemia type 3, hypomagnesemia 3, renal, hypomagnesemia, familial, with hypercalciuria and nephrocalcinosis, hypomagnesemia, familial, with hypercalciuria and nephrocalcinosis hypercalciuria, childhood, self-limiting, included.

Category: General

Looking into renal hypomagnesemia 3? See the lab tests healthcare providers may use to investigate renal hypomagnesemia 3, and learn what each one measures.
Explore tests for renal hypomagnesemia 3
Symptoms

Symptoms associated with renal hypomagnesemia 3

The following symptoms have been associated with renal hypomagnesemia 3 in medical literature. Not everyone experiences the same symptoms.

Tests

Tests used to investigate renal hypomagnesemia 3

Healthcare providers may order these tests when evaluating renal hypomagnesemia 3. 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 renal hypomagnesemia 3, which is why a clinical evaluation is important.

FAQ

Frequently Asked Questions

What is renal hypomagnesemia 3?

renal hypomagnesemia 3 is a health condition described in medical literature. Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement (FHHN) is a form of familial primary hypomagnesemia (FPH), characterized by recurrent urinary tract infections, nephrolithiasis, bilateral nephrocalcinosis, renal magnesium (Mg) wasting, hypercalciuria and kidney failure.

What are the symptoms of renal hypomagnesemia 3?

renal hypomagnesemia 3 is associated with 9 symptoms in the medical literature we index, including Abdominal pain, Failure to thrive, Hematuria, Hypertension, Hypocalcemic seizures, Microscopic hematuria. Symptoms vary widely between individuals.

How is renal hypomagnesemia 3 diagnosed or investigated?

A healthcare provider may use a combination of medical history, physical examination, and tests. Common tests associated with renal hypomagnesemia 3 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 renal hypomagnesemia 3, please discuss your symptoms with a qualified healthcare provider.

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