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Published on: 8/18/2026
Delayed fontanelle closure, when a baby's soft spot stays open past about 18 to 24 months, can reflect normal variation but may also signal congenital hypothyroidism, rickets or vitamin D deficiency, increased intracranial pressure or hydrocephalus, malnutrition, Down syndrome, or skeletal conditions like achondroplasia and cleidocranial dysplasia. Because each of these causes carries very different urgency and testing needs, there are several important factors to consider before assuming it is harmless, and those details are explained below.
If you are worried about your child's soft spot, head shape, or growth milestones, the fastest way to sort a likely benign variation from something needing prompt evaluation is to review the specific symptoms appearing alongside it. A free, instant, online symptom check can help you organize what you are seeing, understand which possible causes fit best, and know what to raise with your pediatrician. Taking a few minutes now can save weeks of uncertainty and help you walk into the next appointment with clear, useful questions.
Last reviewed for medical accuracy: 08/18/2026
A fontanelle—often called the “soft spot”—is a gap between an infant’s skull bones. It lets the baby’s head pass through the birth canal more easily and allows quick brain growth. There are two main fontanelles:
By 18 months of age, most babies’ anterior fontanelles close as the skull bones fuse. Posterior fontanelles usually close by 2–3 months.
When these areas stay open beyond the typical timeframe, it’s called delayed closure of fontanelle.
| Fontanelle | Typical Closure Age | Delayed Closure Defined As… |
|---|---|---|
| Posterior | 2 – 3 months | Still open after 4 months |
| Anterior | 9 – 18 months | Still open after 24 months |
Some healthy infants simply take longer. However, prolonged opening can signal an underlying issue.
Normal Variation
Hypothyroidism (Underactive Thyroid)
Rickets (Vitamin D Deficiency)
Genetic or Chromosomal Conditions
Metabolic Bone Disorders
Increased Intracranial Pressure
Nutritional Factors
Most babies with delayed closure of fontanelle are healthy, but see a healthcare provider if you notice:
If you’re ever unsure, you might consider a free, online symptom check, using the doctor approved Ubie Symptom Checker to help guide your next steps.
Physical Examination
Growth and Development Assessment
Blood Tests
Imaging Studies
Genetic Testing
Treatment depends on the underlying cause:
Normal Variation:
Hypothyroidism:
Rickets:
Genetic/Chromosomal Conditions:
Hydrocephalus:
Nutritional Support:
Regular follow-up helps track improvement and adjust treatment. Your pediatrician will guide you on the best schedule for repeat exams and tests.
Contact a healthcare provider or emergency services if your child has any of the following:
These could indicate life-threatening conditions.
Beyond medical treatment, you can support normal development by:
Early intervention services can help if you spot delays in motor skills, speech or social interaction.
If you’re ever uncertain about your child’s symptoms, consider a free, online symptom check, using the doctor approved Ubie Symptom Checker. Always speak to a doctor about anything that could be life-threatening or serious. Your pediatrician is your best resource for guidance, reassurance and treatment options.
(References)
* Kabbani H, Raghuveer TS. Craniosynostosis. Am Fam Physician. 2004 Jun 15;69(12):2863-70. PMID: 15222651.
* Rizvi R, Anjum Q. Hydrocephalus in children. J Pak Med Assoc. 2005 Nov;55(11):502-7. PMID: 16304873.
* Kalra R, Walker ML. Posterior plagiocephaly. Childs Nerv Syst. 2012 Sep;28(9):1389-93. doi: 10.1007/s00381-012-1784-y. 2012 Aug 8. PMID: 22872253.
* Ma HW. [Rickets-like genetic diseases]. Zhongguo Dang Dai Er Ke Za Zhi. 2013 Nov;15(11):923-7. PMID: 24229581.
* Lattanzi W, Barba M, Di Pietro L, Boyadjiev SA. Genetic advances in craniosynostosis. Am J Med Genet A. 2017 May;173(5):1406-1429. doi: 10.1002/ajmg.a.38159. 2017 Feb 4. PMID: 28160402; PMCID: PMC5397362.
* Kajdic N, Spazzapan P, Velnar T. Craniosynostosis - Recognition, clinical characteristics, and treatment. Bosn J Basic Med Sci. 2018 May 20;18(2):110-116. doi: 10.17305/bjbms.2017.2083. 2018 May 20. PMID: 28623672; PMCID: PMC5988529.
* 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. 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. 2021 Dec 15. PMID: 34910242; PMCID: PMC9307538.
* Stanton E, Urata M, Chen JF, Chai Y. The clinical manifestations, molecular mechanisms and treatment of craniosynostosis. Dis Model Mech. 2022 Apr 1;15(4). doi: 10.1242/dmm.049390. 2022 Apr 22. PMID: 35451466; PMCID: PMC9044212.
* 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. 2025 Apr 10. PMID: 40210850.
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