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Published on: 8/18/2026
Height increases only while the epiphyseal growth plates at the ends of long bones remain open, so when cartilage there is damaged by injury, infection, radiation, chronic inflammation, malnutrition, hormone imbalances such as low growth hormone or untreated hypothyroidism, or premature closure from early puberty, linear growth slows or stops even if the rest of the body appears healthy. Plotting serial heights on a growth chart is the key first step, because crossing downward through percentile lines, a growth velocity under roughly 5 cm per year in mid-childhood, or a height far below the mid-parental target signals a problem worth investigating rather than simply "late blooming." Typical next steps include a bone age X-ray of the hand and wrist to see how much plate cartilage is left, plus blood work for thyroid, IGF-1, celiac disease, kidney function, and puberty-related hormones, since some causes are fully treatable when caught before the plates fuse. Timing matters enormously, and there are several other factors to consider, including limb-length asymmetry after a plate fracture, so review the complete details below before assuming growth has finished.
Because the window for effective treatment closes when the growth plates do, it helps to organize your observations now instead of waiting for the next routine visit, and a free, instant, online symptom check can help you clarify which patterns you are seeing, what questions to bring to a clinician, and how urgently to seek an evaluation.
Last reviewed for medical accuracy: 08/18/2026
When children don’t get enough vitamin D, calcium or phosphate, their bones can’t harden properly. Over time, this leads to soft, weak bones and changes in how the growth plates (epiphyses) function. One of the most visible consequences is short stature and stunted growth from untreated rickets. If you suspect your child’s growth is slowing or if you’ve noticed bowed legs or delayed milestones, understanding how to assess growth and what to do next is crucial.
Epiphyseal growth plates are areas of developing cartilage near the ends of long bones (e.g., femur, tibia). These plates are responsible for:
When these plates are healthy, children grow in predictable patterns. When they’re impaired—by nutritional deficiencies, endocrine disorders or genetic conditions—height gain slows or stops.
Rickets is a condition where bones fail to mineralize properly due to vitamin D deficiency (most common), calcium deficiency or phosphate imbalance. Left untreated, rickets leads to:
Because the growth plates can’t mineralize correctly, the process of new bone formation slows. This directly causes short stature and stunted growth from untreated rickets.
Growth charts are simple, yet powerful tools for tracking a child’s height over time. Accurate measurement and interpretation can reveal early signs of impairment.
Measure correctly
Plot on standardized charts
Track growth velocity
Consider family height
If growth charts show a consistent drop or if current height is well below the mid-parental height range, further evaluation is essential.
When impaired growth is noted, a stepwise approach helps identify and treat underlying causes:
• Clinical history and exam
– Dietary history: intake of vitamin D, calcium-rich foods, milk.
– Sun exposure: limited outdoor time can reduce vitamin D synthesis.
– Developmental milestones and bone pain.
– Physical exam: look for bone deformities, muscle tone, dental enamel defects.
• Laboratory tests
– 25-hydroxyvitamin D: <20 ng/mL suggests deficiency.
– Serum calcium and phosphate: low levels support rickets.
– Alkaline phosphatase (ALP): high in active rickets.
– Parathyroid hormone (PTH): elevated when calcium is low.
– Kidney function tests: rule out renal causes of rickets.
• Imaging studies
– Wrist and knee X-rays: show classic metaphyseal changes (cupping, fraying).
– Bone age assessment: delayed bone age confirms growth delay.
• Referral considerations
– Pediatric endocrinologist: if hormone disorders are suspected.
– Pediatric orthopedic surgeon: for severe deformities that may need bracing or surgery.
– Registered dietitian: to develop a balanced, nutrient-rich diet plan.
Correcting rickets and helping growth plates resume normal function involves:
Nutritional therapy
Sunlight exposure
Monitoring and follow-up
Orthopedic management
Early and consistent treatment often allows growth plates to recover, reducing long-term height deficits. The earlier you catch rickets, the better the outcome.
Rickets itself isn’t typically life-threatening, but if you notice any of the following, speak to a doctor promptly:
For a quick assessment of symptoms, consider a free, online symptom check, using the doctor approved Ubie Symptom Checker. This tool can help guide your next steps and prepare you for a visit with your healthcare provider.
Impaired epiphyseal growth plates, especially due to untreated rickets, directly lead to short stature and stunted growth. By tracking growth on standardized charts, ordering appropriate labs and imaging, and initiating nutritional and orthopedic treatments, most children can catch up in growth. Early detection is key—watch for drops in growth percentiles, bone pain or deformities. If anything seems serious or life-threatening, always speak to a doctor for personalized advice and care.
(References)
* Boersma B, Wit JM. Catch-up growth. Endocr Rev. 1997 Oct;18(5):646-61. doi: 10.1210/edrv.18.5.0313. PMID: 9331546.
* Simm PJ, Bajpai A, Russo VC, Werther GA. Estrogens and growth. Pediatr Endocrinol Rev. 2008 Sep;6(1):32-41. PMID: 18806723.
* Santos F, Fuente R, Mejia N, Mantecon L, Gil-Peña H, Ordoñez FA. Hypophosphatemia and growth. Pediatr Nephrol. 2013 Apr;28(4):595-603. doi: 10.1007/s00467-012-2364-9. Epub 2012 Nov 22. PMID: 23179196.
* Baron J, Sävendahl L, De Luca F, Dauber A, Phillip M, Wit JM, Nilsson O. Short and tall stature: a new paradigm emerges. Nat Rev Endocrinol. 2015 Dec;11(12):735-46. doi: 10.1038/nrendo.2015.165. Epub 2015 Oct 6. PMID: 26437621; PMCID: PMC5002943.
* Jee YH, Baron J. The Biology of Stature. J Pediatr. 2016 Jun;173:32-8. doi: 10.1016/j.jpeds.2016.02.068. Epub 2016 Mar 26. PMID: 27025909; PMCID: PMC4884478.
* Fuente R, Gil-Peña H, Claramunt-Taberner D, Hernández O, Fernández-Iglesias A, Alonso-Durán L, Rodríguez-Rubio E, Santos F. X-linked hypophosphatemia and growth. Rev Endocr Metab Disord. 2017 Mar;18(1):107-115. doi: 10.1007/s11154-017-9408-1. PMID: 28130634.
* Jee YH, Andrade AC, Baron J, Nilsson O. Genetics of Short Stature. Endocrinol Metab Clin North Am. 2017 Jun;46(2):259-281. doi: 10.1016/j.ecl.2017.01.001. Epub 2017 Feb 23. PMID: 28476223; PMCID: PMC5424617.
* Linglart A, Merzoug V, Lambert AS, Adamsbaum C. Bone dysplasia. Ann Endocrinol (Paris). 2017 Jun;78(2):114-122. doi: 10.1016/j.ando.2017.04.011. Epub 2017 May 8. PMID: 28495326.
* Grimberg A, Hawkes CP. Growth Hormone Treatment for Non-GHD Disorders: Excitement Tempered by Biology. J Clin Endocrinol Metab. 2024 Jan 18;109(2):e442-e454. doi: 10.1210/clinem/dgad417. PMID: 37450564; PMCID: PMC10795916.
* Cohen LE, Rogol AD. Children With Idiopathic Short Stature: An Expanding Role for Genetic Investigation in Their Medical Evaluation. Endocr Pract. 2024 Jul;30(7):679-686. doi: 10.1016/j.eprac.2024.04.009. Epub 2024 Apr 26. PMID: 38679385.
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