Familial hypocalciuric hypercalcemia (patient information): Difference between revisions

	Familial hypocalciuric hypercalcemia
Overview
What are the symptoms?
What are the causes?
Who is at highest risk?
Diagnosis
When to seek urgent medical care?
Treatment options
Where to find medical care for Familial hypocalciuric hypercalcemia?
Prevention
What to expect (Outlook/Prognosis)?
Possible complications
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Latest revision as of 14:48, 16 October 2017

For the WikiDoc page for this topic, click here

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Ajay Gade MD [2]]

Overview

Familial hypocalciuric hypercalcemia is a genetic condition characterized by asymptomatic hypercalcemia and low urinary calcium.

What are the Symptoms of Familial hypocalciuric hypercalcemia?

The majority of patients with familial hypocalciuric hypercalcemia (FHH) are asymptomatic.However, FHH can present with signs and symptoms of hypercalcemia such as:

What Causes Familial hypocalciuric hypercalcemia?

FHH is a benign inherited condition caused by mutations in the calcium-sensing receptor located on chromosome 3.
The calcium-sensing receptor is present on the parathyroid glands that are present in the neck region and the lining the kidney tubule.
CASR has the ability to sense small changes in circulating calcium concentration and send this information that modifies parathyroid hormone (PTH) secretion or renal calcium handling.
Inherited abnormalities of the CASR gene, can cause either hypercalcemia or hypocalcemia depending upon whether they are inactivating or activating.

Who is at Highest Risk?

Patients with a positive family history of high blood calcium and absence of symptoms are at high risk.

Diagnosis

Blood tests are done to check for increased levels of calcium, phosphate, parathyroid hormone (PTH), and alkaline phosphatase. A 24-hour urine collection test can help determine how much calcium is being removed from the body.

Bone x-rays and bone mineral density test can help detect bone loss, fractures, or bone softening.

X-rays, ultrasound, or CT scans of the kidneys or urinary tract may show calcium deposits or a blockage.

When to Seek Urgent Medical Care?

Make an appointment with your primary care physician if you have any symptoms of hypercalcemia.

Treatment Options

There is no treatment for FHH as it is a benign condition. Surgical intervention is not recommended for the FHH, rarely parathyroid glands are removed by surgical excision in patients with associated conditions such as

Where to find Medical Care for Familial hypocalciuric hypercalcemia?

Make an appointment with your primary care physician if you have symptoms of hypercalcemia.

Prevention

There are no established measures for the primary or secondary prevention of familial hypocalciuric hypercalcemia.

What to Expect (Outlook/Prognosis)?

This is an asymptomatic condition. People with this condition can have a normal lifespan with a routine lifestyle.

Possible Complications

Very rarely FHH can cause complications secondary to hypercalcemia, which includes:

Urinary tract infection due to kidney stones and blockage
Peptic ulcer disease
Pancreatitis
Pseudogout

Sources

Template:WH Template:WS

@@ Line 3: / Line 3: @@
 '''For the WikiDoc page for this topic, click [[Familial hypocalciuric hypercalcemia|here]]'''
-{{CMG}}; {{AE}}
+{{CMG}}; {{AE}}{{Ajay}}
 ==Overview==
-Familial hypocalciuric hypercalcemia is an autosomal dominant inherited disorder characterized by asymptomatic hypercalcemia and low urinary calcium.
+[[Familial hypocalciuric hypercalcemia]] is a genetic condition characterized by asymptomatic hypercalcemia and low urinary calcium.
 ==What are the Symptoms of Familial hypocalciuric hypercalcemia?==
-The majority of patients with FHH are asymptomatic.However, FHH can present with signs and symptoms of hypercalcemia such as:
+The majority of patients with familial hypocalciuric hypercalcemia (FHH) are asymptomatic.However, FHH can present with signs and symptoms of [[hypercalcemia]] such as:
 * [[Constipation]]
-* [[Polyuria]]
+* [[Increased urination]]
-* [[Polydipsia]]
+* [[Polydipsia|Increased thirst]]
-* [[Anorexia]]
+* [[Loss of appetite]]
-* [[Anhedonia]]
+* Loss of concentration
-* Abdominal pain
+* [[Abdominal pain]]
 * [[Muscle weakness]]
 * [[Confusion]]
 * [[Fatigue]]
-* Neuropsychiatric symptoms<ref name="pmid20059346">{{cite journal |vauthors=Whitcomb DC |title=Genetic aspects of pancreatitis |journal=Annu. Rev. Med. |volume=61 |issue= |pages=413–24 |year=2010 |pmid=20059346 |doi=10.1146/annurev.med.041608.121416 |url=}}</ref>.
+* [[Neuropsychiatric|Neuropsychiatric symptoms]]
 ==What Causes Familial hypocalciuric hypercalcemia?==
-FHH is an autosomal dominant benign inherited condition caused by inactivating missense mutation of the CASR located on chromosome 3q<ref name="pmid25104082">{{cite journal |vauthors=Stratta P, Merlotti G, Musetti C, Quaglia M, Pagani A, Izzo C, Radin E, Airoldi A, Baorda F, Palladino T, Leone MP, Guarnieri V |title=Calcium-sensing-related gene mutations in hypercalcaemic hypocalciuric patients as differential diagnosis from primary hyperparathyroidism: detection of two novel inactivating mutations in an Italian population |journal=Nephrol. Dial. Transplant. |volume=29 |issue=10 |pages=1902–9 |year=2014 |pmid=25104082 |doi=10.1093/ndt/gfu065 |url=}}</ref><ref name="pmid26963950">{{cite journal |vauthors=Vargas-Poussou R, Mansour-Hendili L, Baron S, Bertocchio JP, Travers C, Simian C, Treard C, Baudouin V, Beltran S, Broux F, Camard O, Cloarec S, Cormier C, Debussche X, Dubosclard E, Eid C, Haymann JP, Kiando SR, Kuhn JM, Lefort G, Linglart A, Lucas-Pouliquen B, Macher MA, Maruani G, Ouzounian S, Polak M, Requeda E, Robier D, Silve C, Souberbielle JC, Tack I, Vezzosi D, Jeunemaitre X, Houillier P |title=Familial Hypocalciuric Hypercalcemia Types 1 and 3 and Primary Hyperparathyroidism: Similarities and Differences |journal=J. Clin. Endocrinol. Metab. |volume=101 |issue=5 |pages=2185–95 |year=2016 |pmid=26963950 |doi=10.1210/jc.2015-3442 |url=}}</ref>.
+* FHH is a benign inherited condition caused by mutations in the calcium-sensing receptor located on chromosome 3.
-There are three types of FHH
+* The calcium-sensing receptor is present on the [[Parathyroid gland|parathyroid glands]] that are present in the neck region and the lining the kidney tubule.
-* Type-1: caused by loss-of-function mutations of the calcium-sensing receptor (CaSR), a G-protein coupled receptor that predominantly signals via G-protein subunit alpha-11 (Gα11) to regulate calcium homeostasis located on chromosome 3q13.3-q21<ref name="pmid26729423">{{cite journal |vauthors=Gorvin CM, Cranston T, Hannan FM, Rust N, Qureshi A, Nesbit MA, Thakker RV |title=A G-protein Subunit-α11 Loss-of-Function Mutation, Thr54Met, Causes Familial Hypocalciuric Hypercalcemia Type 2 (FHH2) |journal=J. Bone Miner. Res. |volume=31 |issue=6 |pages=1200–6 |year=2016 |pmid=26729423 |pmc=4949650 |doi=10.1002/jbmr.2778 |url=}}</ref><ref name="pmid23802516">{{cite journal |vauthors=Nesbit MA, Hannan FM, Howles SA, Babinsky VN, Head RA, Cranston T, Rust N, Hobbs MR, Heath H, Thakker RV |title=Mutations affecting G-protein subunit α11 in hypercalcemia and hypocalcemia |journal=N. Engl. J. Med. |volume=368 |issue=26 |pages=2476–2486 |year=2013 |pmid=23802516 |pmc=3773604 |doi=10.1056/NEJMoa1300253 |url=}}</ref>.
+* CASR has the ability to sense small changes in circulating calcium concentration and send this information that modifies [[PTH|parathyroid hormone (PTH)]] secretion or renal calcium handling.
-* Type-2: caused by heterozygous mutation in the GNA11 gene on chromosome 19p13<ref name="pmid28176280">{{cite journal |vauthors=Szalat A, Shpitzen S, Tsur A, Zalmon Koren I, Shilo S, Tripto-Shkolnik L, Durst R, Leitersdorf E, Meiner V |title=Stepwise CaSR, AP2S1, and GNA11 sequencing in patients with suspected familial hypocalciuric hypercalcemia |journal=Endocrine |volume=55 |issue=3 |pages=741–747 |year=2017 |pmid=28176280 |doi=10.1007/s12020-017-1241-5 |url=}}</ref>.
+* Inherited abnormalities of the CASR gene, can cause either [[hypercalcemia]] or [[hypocalcemia]] depending upon whether they are inactivating or activating.
-* Type-3: caused by heterozygous mutation in the AP2S1 gene on chromosome 19q13<ref name="pmid24731014">{{cite journal |vauthors=Hendy GN, Canaff L, Newfield RS, Tripto-Shkolnik L, Wong BY, Lee BS, Cole DE |title=Codon Arg15 mutations of the AP2S1 gene: common occurrence in familial hypocalciuric hypercalcemia cases negative for calcium-sensing receptor (CASR) mutations |journal=J. Clin. Endocrinol. Metab. |volume=99 |issue=7 |pages=E1311–5 |year=2014 |pmid=24731014 |doi=10.1210/jc.2014-1120 |url=}}</ref><ref name="pmid26646938">{{cite journal |vauthors=Mayr B, Schnabel D, Dörr HG, Schöfl C |title=GENETICS IN ENDOCRINOLOGY: Gain and loss of function mutations of the calcium-sensing receptor and associated proteins: current treatment concepts |journal=Eur. J. Endocrinol. |volume=174 |issue=5 |pages=R189–208 |year=2016 |pmid=26646938 |doi=10.1530/EJE-15-1028 |url=}}</ref>.
-===Genetic Causes===
+==Who is at Highest Risk?==
-*FHH is caused by a mutation in the CASR gene located on chromosome 3<ref name="pmid11013439">{{cite journal |vauthors=Hendy GN, D'Souza-Li L, Yang B, Canaff L, Cole DE |title=Mutations of the calcium-sensing receptor (CASR) in familial hypocalciuric hypercalcemia, neonatal severe hyperparathyroidism, and autosomal dominant hypocalcemia |journal=Hum. Mutat. |volume=16 |issue=4 |pages=281–96 |year=2000 |pmid=11013439 |doi=10.1002/1098-1004(200010)16:4<281::AID-HUMU1>3.0.CO;2-A |url=}}</ref>.
+Patients with a positive family history of high blood calcium and absence of symptoms are at high risk.
-* The calcium-sensing receptor is a plasma membrane G protein-coupled receptor that is expressed on the chief cells of the parathyroid gland and the lining the kidney tubule.
-* CASR has the ability to sense small changes in circulating calcium concentration and send this information to intracellular signaling pathways that modify PTH secretion or renal calcium handling.
-* Inherited abnormalities of the CASR gene located on chromosome 3p13.3-21 can cause either hypercalcemia or hypocalcemia depending upon whether they are inactivating or activating.
-* Heterozygous loss-of-functional mutations give rise to FHH, a lifelong asymptomatic hypercalcemia.
-* The homozygous condition manifests as neonatal severe hyperparathyroidism, a rare disorder characterized by extreme hypercalcemia and the bony changes of hyperparathyroidism.
-* The disorder autosomal dominant hypocalcemia is due to gain-of-function mutations in the CASR gene, this can be asymptomatic or presents with seizures.
-* A common polymorphism in the intracellular tail of the CASR, Ala to Ser at position 986, has a modest effect on the serum calcium concentration in healthy individuals<ref name="pmid11013439">{{cite journal |vauthors=Hendy GN, D'Souza-Li L, Yang B, Canaff L, Cole DE |title=Mutations of the calcium-sensing receptor (CASR) in familial hypocalciuric hypercalcemia, neonatal severe hyperparathyroidism, and autosomal dominant hypocalcemia |journal=Hum. Mutat. |volume=16 |issue=4 |pages=281–96 |year=2000 |pmid=11013439 |doi=10.1002/1098-1004(200010)16:4<281::AID-HUMU1>3.0.CO;2-A |url=}}</ref><ref name="pmid15241791">{{cite journal |vauthors=Pidasheva S, D'Souza-Li L, Canaff L, Cole DE, Hendy GN |title=CASRdb: calcium-sensing receptor locus-specific database for mutations causing familial (benign) hypocalciuric hypercalcemia, neonatal severe hyperparathyroidism, and autosomal dominant hypocalcemia |journal=Hum. Mutat. |volume=24 |issue=2 |pages=107–11 |year=2004 |pmid=15241791 |doi=10.1002/humu.20067 |url=}}</ref><ref name="pmid15662592">{{cite journal |vauthors=Felderbauer P, Hoffmann P, Klein W, Bulut K, Ansorge N, Epplen JT, Schmitz F, Schmidt WE |title=Identification of a novel calcium-sensing receptor gene mutation causing familial hypocalciuric hypercalcemia by single-strand conformation polymorphism analysis |journal=Exp. Clin. Endocrinol. Diabetes |volume=113 |issue=1 |pages=31–4 |year=2005 |pmid=15662592 |doi=10.1055/s-2004-830523 |url=}}</ref>.
-==Who is at Highest Risk?==
+==Diagnosis==
+Blood tests are done to check for increased levels of [[calcium]], [[phosphate]], [[parathyroid hormone]] (PTH),  and [[alkaline phosphatase]]. A 24-hour urine collection test can help determine how much calcium is being removed from the body.
+Bone [[x-rays]] and bone mineral density test can help detect [[bone loss]], [[fractures]], or bone softening.
-==Diagnosis==
+[[X-rays|X-rays,]] [[ultrasound]], or [[CT scan]]<nowiki/>s of the [[kidneys]] or [[Urinary system|urinary tract]] may show calcium deposits or a blockage.
 ==When to Seek Urgent Medical Care?==
+Make an appointment with your [[primary care physician]] if you have any symptoms of hypercalcemia.
 ==Treatment Options==
-==Medical Therapy==
+There is no treatment for FHH as it is a benign condition.
-There is no treatment for FHH as it is a benign condition. However, the avoidance of parathyroidectomy should be emphasized to the FHH diagnosed patients<ref name="pmid3977197">{{cite journal |vauthors=Law WM, Heath H |title=Familial benign hypercalcemia (hypocalciuric hypercalcemia). Clinical and pathogenetic studies in 21 families |journal=Ann. Intern. Med. |volume=102 |issue=4 |pages=511–9 |year=1985 |pmid=3977197 |doi= |url=}}</ref><ref name="pmid2673770">{{cite journal |vauthors=Heath H |title=Familial benign (hypocalciuric) hypercalcemia. A troublesome mimic of mild primary hyperparathyroidism |journal=Endocrinol. Metab. Clin. North Am. |volume=18 |issue=3 |pages=723–40 |year=1989 |pmid=2673770 |doi= |url=}}</ref>.
+Surgical intervention is not recommended for the FHH, rarely [[parathyroid glands]] are removed by surgical excision in patients with associated conditions such as
-==Surgery==
-Surgical intervention is not recommended for the management of FHH.
-===Indications===
-Parathyroidectomy in FHH is rarely done in patients if associated conditions are present along with the FHH such as<ref name="pmid19423559">{{cite journal |vauthors=Brachet C, Boros E, Tenoutasse S, Lissens W, Andry G, Martin P, Bergmann P, Heinrichs C |title=Association of parathyroid adenoma and familial hypocalciuric hypercalcaemia in a teenager |journal=Eur. J. Endocrinol. |volume=161 |issue=1 |pages=207–10 |year=2009 |pmid=19423559 |doi=10.1530/EJE-09-0257 |url=}}</ref><ref name="pmid10843194">{{cite journal |vauthors=Carling T, Szabo E, Bai M, Ridefelt P, Westin G, Gustavsson P, Trivedi S, Hellman P, Brown EM, Dahl N, Rastad J |title=Familial hypercalcemia and hypercalciuria caused by a novel mutation in the cytoplasmic tail of the calcium receptor |journal=J. Clin. Endocrinol. Metab. |volume=85 |issue=5 |pages=2042–7 |year=2000 |pmid=10843194 |doi=10.1210/jcem.85.5.6477 |url=}}</ref>
 * [[Parathyroid adenoma]]
 * [[Pancreatitis]]
 * [[Hyperparathyroidism]]
-* Hypercalciuria
+* [[Hypercalciuria]]
 ==Where to find Medical Care for Familial hypocalciuric hypercalcemia?==
-Call for an appointment with your healthcare provider if you have symptoms of hypercalcemia.
+Make an appointment with your primary care physician if you have symptoms of hypercalcemia.
 ==Prevention==
@@ Line 67: / Line 55: @@
 ==What to Expect (Outlook/Prognosis)?==
+This is an asymptomatic condition. People with this condition can have a normal lifespan with a routine lifestyle.
 ==Possible Complications==
+Very rarely FHH can cause complications secondary to hypercalcemia, which includes:
+* [[Urinary tract infection]] due to [[Kidney stone|kidney stones]] and blockage
+* [[Peptic ulcer disease]]
+* [[Pancreatitis]]
+* [[Pseudogout]]
 ==Sources==
-http://www.nlm.nih.gov/medlineplus/ency/article/000434.htm
 {{WH}}
 {{WS}}
+<references />