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Published on: 8/18/2026
A fontanelle that stays open past the typical window (about 2 to 3 months for the back soft spot and 12 to 24 months for the front) is often a harmless variation, but it can sometimes point to hypothyroidism, vitamin D deficiency or rickets, raised intracranial pressure or hydrocephalus, or a genetic condition, so the questions you raise at the next visit matter. Useful things to ask include: how has head circumference tracked on the growth curve, is the soft spot flat, bulging, or sunken, are developmental milestones on time, is vitamin D and feeding intake adequate, were newborn thyroid screening results normal, and would blood tests or imaging be worthwhile now or at a follow-up. There are several factors that change how urgent this is, including your child's age, growth pattern, and any other symptoms, so review the complete details below before deciding what to do next.
Because open fontanelles can look identical whether the cause is benign or something treatable, a quick, free, and anonymous online symptom check can help you organize what you are noticing into clear, specific concerns. It takes only a few minutes, flags whether your observations suggest a need for prompt evaluation, and gives you a focused list of questions and possible causes to bring to your pediatrician so nothing important gets overlooked.
Last reviewed for medical accuracy: 08/18/2026
Fontanelles—often called “soft spots”—are gaps between an infant’s skull bones. They allow the brain to grow quickly in the first year of life. Most front (anterior) fontanelles close by 18–24 months. If closure happens later, it’s called delayed closure of fontanelle. This guide helps you understand what to ask your doctor, why it matters, and when to seek further evaluation.
Delayed closure alone is often harmless. Bone growth can vary slightly from child to child. Still, it can sometimes hint at underlying conditions.
Normal variation
• Some healthy children simply have a slightly later closure.
• Family history of similar timing may be reassuring.
Nutritional factors
• Rickets (vitamin D deficiency) can soften bones.
• Poor calcium intake or absorption.
Genetic conditions
• Down syndrome
• Cleidocranial dysplasia (impacts bone formation)
Endocrine disorders
• Hypothyroidism (low thyroid hormone)
• Growth hormone deficiency
Chromosomal anomalies
• Certain syndromes affect skull bone development.
Metabolic bone diseases
• Osteogenesis imperfecta (“brittle bone disease”)
Asking targeted questions helps you and your child’s doctor determine:
Approach your pediatrician or family doctor prepared with questions. This ensures you cover all key points.
Use this checklist when you talk with your child’s medical provider:
Most cases of delayed closure of fontanelle turn out to be benign. However, prompt attention is vital if you notice any of the following:
If these symptoms appear, speak to a doctor right away or seek emergency care.
When you and your pediatrician decide on evaluation, common steps include:
Physical exam
• Measure fontanelle size and inspect skull shape.
• Check for other signs of bone or endocrine issues.
Blood tests
• Calcium, phosphate, alkaline phosphatase (rickets markers)
• Thyroid hormone levels
• Vitamin D levels
Imaging
• Skull X-ray to view bone edges.
• In rare cases, CT scan for detailed bone structure.
Genetic testing
• If a genetic syndrome is suspected.
• Family history guides which tests to order.
Treatment depends on the underlying cause:
Early intervention can help ensure normal growth and development.
If you’re still uncertain about your child’s symptoms or need to prioritize concerns, you might consider a free, online symptom check, using the doctor approved Ubie Symptom Checker. This tool can help you sort through possible causes and decide if you should see a doctor soon.
Delayed fontanelle closure rarely indicates a life-threatening condition, but proper evaluation is crucial. Always speak to a doctor if your child has:
Your child’s health is too important to leave to chance. If you ever worry your child needs immediate care, call your pediatrician or visit an emergency department without delay.
(References)
* Gorlin RJ, Whitley CB. Lenz-Majewski syndrome. Radiology. 1983 Oct;149(1):129-31. doi: 10.1148/radiology.149.1.6611917. PMID: 6611917.
* Rizvi R, Anjum Q. Hydrocephalus in children. J Pak Med Assoc. 2005 Nov;55(11):502-7. PMID: 16304873.
* Angelieri F, Cevidanes LH, Franchi L, Gonçalves JR, Benavides E, McNamara JA Jr. Midpalatal suture maturation: classification method for individual assessment before rapid maxillary expansion. Am J Orthod Dentofacial Orthop. 2013 Nov;144(5):759-69. doi: 10.1016/j.ajodo.2013.04.022. PMID: 24182592; PMCID: PMC4185298.
* Ma HW. [Rickets-like genetic diseases]. Zhongguo Dang Dai Er Ke Za Zhi. 2013 Nov;15(11):923-7. PMID: 24229581.
* Xing C, Kanchwala M, Rios JJ, Hyatt T, Wang RC, Tran A, Dougherty I, Tovar-Garza A, Purnadi C, Kumar MG, Berk D, Shinawi M, Irvine AD, Toledo-Bahena M, Agim NG, Glass DA 2nd. Biallelic variants in RNU12 cause CDAGS syndrome. Hum Mutat. 2021 Aug;42(8):1042-1052. doi: 10.1002/humu.24239. Epub 2021 Jun 15. PMID: 34085356.
* Haffner D, Leifheit-Nestler M, Grund A, Schnabel D. Rickets guidance: part I-diagnostic workup. Pediatr Nephrol. 2022 Sep;37(9):2013-2036. doi: 10.1007/s00467-021-05328-w. Epub 2021 Dec 15. PMID: 34910242; PMCID: PMC9307538.
* Lally S, Walsh N, Kenny J, Franklin O, Cotter M, Richardson S, McEligott F, Finan A. Fontaine progeroid syndrome-A case report. Clin Case Rep. 2022 Sep;10(9):e6291. doi: 10.1002/ccr3.6291. Epub 2022 Sep 6. PMID: 36093452; PMCID: PMC9448962.
* Adam MP, Bick S, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, Cheng S, Lo IFM, Luk HM. FAM111A-Related Skeletal Dysplasias. 1993. PMID: 37023242.
* Alperovich M, Tonello C, Mayes LC, Kahle KT. Non-syndromic craniosynostosis. Nat Rev Dis Primers. 2025 Apr 10;11(1):24. doi: 10.1038/s41572-025-00607-4. Epub 2025 Apr 10. PMID: 40210850.
* Adam MP, Bick S, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, Kosho T, Yamaguchi T, Mizumoto S, Mendoza-Londono R. Musculocontractural Ehlers-Danlos Syndrome. 1993. PMID: 40373179.
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