What Are Low Calcium Symptoms in 22q11.2 Deletion?
At a Glance
Children with 22q11.2 deletion syndrome often experience low blood calcium (hypocalcemia) due to underdeveloped parathyroid glands. Early symptoms include tingling in the fingers or mouth and muscle cramps. Severe signs like locked muscle spasms, breathing issues, or seizures require emergency care.
Children with 22q11.2 deletion syndrome often experience hypocalcemia (low levels of calcium in the blood), which can cause invisible but dangerous complications [1]. This happens because the parathyroid glands—four tiny glands in the neck that control calcium levels—often do not develop properly before birth [1][2]. Without fully functioning parathyroid glands, your child’s body struggles to keep enough calcium in their blood, a condition known as hypoparathyroidism [3].
Low calcium can happen at any age, even if your child has previously had normal calcium levels [4]. Because a severe low calcium episode can become a medical emergency, it is crucial to know exactly what signs to watch for so you can seek prompt care.
Physical Signs of Low Calcium
The symptoms of a low calcium episode can range from mild to severe, depending on how quickly and how significantly the calcium levels drop. Because young children cannot always explain what they are feeling, parents should watch closely for these physical signs:
- Tingling and Numbness (Paresthesia): This often starts as a “pins and needles” sensation around the mouth, lips, or in the fingers and toes [5][6].
- Muscle Cramps and Pain: You might notice your child complaining of severe muscle aches, stiffness, or spasms, particularly in their legs, arms, or abdomen [7].
- Fatigue and Irritability: While harder to pinpoint, extreme fatigue or sudden changes in mood and irritability can be early warning signs [5].
- Tetany: This is a severe form of muscle spasm where the muscles involuntarily contract and lock. Most commonly, you might see your child’s hands or feet cramp inward in an unnatural position (carpopedal spasms) [8][9].
- Breathing Difficulties: In serious cases, low calcium can cause spasms in the throat (laryngospasm) or airways (bronchospasm), making it hard to breathe [9][10]. This is a medical emergency requiring immediate attention (such as calling 911).
- Seizures: If calcium drops too low, it can trigger generalized convulsions or seizures [9]. This is also a medical emergency requiring immediate medical care.
What Triggers a Low Calcium Episode?
Your child’s body uses more calcium during times of physical or physiological stress. Because underdeveloped parathyroid glands cannot ramp up hormone production to meet this higher demand, blood calcium levels can suddenly plunge [11][12]. Common triggers for a hypocalcemic episode include:
- Illnesses and Infections: Even common childhood viruses or fevers place stress on the body and can deplete calcium stores or trigger an imbalance [12].
- Growth Spurts and Puberty: Periods of rapid skeletal growth, such as during adolescence, require immense amounts of calcium, frequently unmasking hypocalcemia that had previously gone unnoticed [13].
- Surgery: Any surgical procedure is a major physical stressor that can cause a severe drop in calcium [11].
- Certain Medications: Medications sometimes prescribed for children with 22q11.2 deletion syndrome, including specific anti-seizure drugs (like phenytoin) and psychiatric medications, can interfere with calcium balance [14].
Preparing for Episodes
While you cannot always prevent a low calcium episode, you can be prepared. It is vital to work with your child’s medical team to create a proactive action plan. Ask your endocrinologist what specific steps you should take if you notice mild signs (like tingling or muscle cramps), and clarify exactly when you should head to the emergency room versus calling the clinic. Many families find it helpful to establish a “sick-day protocol” for managing routine illnesses, and to carry a standardized emergency care letter to share with school nurses and teachers so that everyone knows how to spot these symptoms early.
Common questions in this guide
What does low calcium feel like for a child?
Why do children with 22q11.2 deletion syndrome get low calcium?
What triggers a sudden drop in calcium levels?
When is a low calcium episode a medical emergency?
How can I prepare for my child's low calcium episodes?
Questions to Ask Your Doctor
Curated prompts to bring to your next appointment.
- 1.What is our specific 'sick-day protocol' for managing my child's calcium levels when they have a common illness, fever, or stomach bug?
- 2.At what point should I call the clinic versus going directly to the emergency room if I notice mild symptoms like tingling or muscle cramps?
- 3.Should we carry an emergency medical letter or create an action plan to share with my child's school and other caregivers?
- 4.How often should we be doing routine blood tests to monitor calcium and parathyroid hormone levels, especially as my child approaches puberty?
- 5.Are any of my child's current medications increasing their risk for a low calcium episode, and are there safer alternatives?
Questions For You
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References
References (14)
- 1
Association of hypocalcemia with congenital heart disease in 22q11.2 deletion syndrome.
Rayannavar A, Levitt Katz LE, Crowley TB, et al.
American journal of medical genetics. Part A 2018; (176(10)):2099-2103 doi:10.1002/ajmg.a.40495.
PMID: 30277015 - 2
Review of the Pathophysiology and Clinical Manifestations of 22q11.2 Deletion and Duplication Syndromes.
Purow J, Waidner L, Ale H
Clinical reviews in allergy & immunology 2025; (68(1)):23 doi:10.1007/s12016-025-09035-4.
PMID: 40038168 - 3
Hypoparathyroidism and late-onset hypogonadism in an adult male with familial 22q11.2 deletion syndrome: a case report with 3-year follow-up and review of the literature.
Chen X, Yang L, Li J, Tan H
BMC endocrine disorders 2022; (22(1)):278 doi:10.1186/s12902-022-01150-z.
PMID: 36371175 - 4
Hypocalcemia due to 22q11.2 deletion syndrome diagnosed in adulthood.
Cabrer M, Serra G, Gogorza MS, Pereg V
Endocrinology, diabetes & metabolism case reports 2018; (2018()) doi:10.1530/EDM-17-0140.
PMID: 29340157 - 5
A Rare Familial Case of Pseudohypoparathyroidism Type 1b in Two Brothers Presenting With Recurrent Leg Cramps and Learning Difficulties.
Yunas HA, Ismail A, Chowdhury EA, et al.
Cureus 2025; (17(12)):e99606 doi:10.7759/cureus.99606.
PMID: 41555976 - 6
Tingles, Tetany, and Electrolyte Derangements.
Singh A, Kaur R, Dass B, Ejaz A
Cureus 2020; (12(4)):e7854 doi:10.7759/cureus.7854.
PMID: 32483505 - 7
[Clinical and genetic characteristics of primary hypoparathyroidism in children].
Song FY, Du M, Dong Q, et al.
Zhonghua er ke za zhi = Chinese journal of pediatrics 2020; (58(11)):917-922 doi:10.3760/cma.j.cn112140-20200317-00258.
PMID: 33120464 - 8
Hypercalcaemia to hypocalcaemia: tetany as a side effect of intravenous bisphosphonate treatment.
Bounds L, McGrath F, Taubert M
BMJ case reports 2022; (15(4)) doi:10.1136/bcr-2022-249141.
PMID: 35487644 - 9
Neurological manifestation of 22q11.2 deletion syndrome.
Bayat M, Bayat A
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2022; (43(3)):1695-1700 doi:10.1007/s10072-021-05825-8.
PMID: 35039989 - 10
Hypomagnesaemia induced hypocalcemia mimicking as acute exacerbation of COPD-Rare cause of a common presentation: A case report.
Roy S, Meena M, Dhoot NB, Kant R
Journal of family medicine and primary care 2020; (9(5)):2541-2543 doi:10.4103/jfmpc.jfmpc_314_20.
PMID: 32754541 - 11
Endocrine Abnormalities and Growth Characterization in Colombian Pediatric Patients with 22q11 Deletion Syndrome
Lasprilla-Tovar J, Zuluaga NA, Forero C, et al.
Journal of clinical research in pediatric endocrinology 2023; (15(1)):16-24 doi:10.4274/jcrpe.galenos.2022.2022-4-12.
PMID: 35984227 - 12
Endocrine and Growth Disorders in Taiwanese Children With 22q11.2 Deletion Syndrome.
Lin HY, Tsai WY, Tung YC, et al.
Frontiers in endocrinology 2022; (13()):771100 doi:10.3389/fendo.2022.771100.
PMID: 35432203 - 13
Delayed diagnosis of 22q11 deletion syndrome due to late onset hypocalcemia in a 11-year-old girl with imperforated anus.
Yoo DY, Kim HJ, Cho KH, et al.
Annals of pediatric endocrinology & metabolism 2017; (22(2)):133-138 doi:10.6065/apem.2017.22.2.133.
PMID: 28690994 - 14
22q11.2 deletion syndrome lowers seizure threshold in adult patients without epilepsy.
Wither RG, Borlot F, MacDonald A, et al.
Epilepsia 2017; (58(6)):1095-1101 doi:10.1111/epi.13748.
PMID: 28448680
This page provides educational information about low calcium symptoms in 22q11.2 deletion syndrome. It does not replace professional medical advice. Always consult your endocrinologist or seek emergency care if you suspect your child is experiencing severe hypocalcemia.
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