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Dent disease
URL of this page: https://medlineplus.gov/genetics/condition/dent-disease/

Dent disease

Description

Dent disease is a chronic kidney disorder that occurs almost exclusively in males. The kidney problems seen in affected individuals are a result of damage to structures called proximal tubules. These structures help reabsorb water, protein, and other nutrients into the bloodstream or release them into the urine.

The signs and symptoms of Dent disease tend to appear in childhood and worsen over time. However, the features and the severity of Dent disease vary greatly among affected individuals.

The most frequent sign of Dent disease is the loss of small proteins in the urine (also called low-molecular-weight or LMW proteinuria). Too much calcium in the urine (hypercalciuria) is another common sign of Dent disease. LMW proteinuria and hypercalciuria may be the only signs of Dent disease in affected children.

Additional signs and symptoms of Dent disease can include calcium deposits in the kidneys (nephrocalcinosis) and kidney stones (nephrolithiasis). Kidney stones can cause abdominal pain and blood in the urine (hematuria). Thirty to 80 percent of people with Dent disease develop kidney failure in early to mid-adulthood. Kidney failure can be life-threatening and occurs when the kidneys are no longer able to effectively filter fluids and waste products from the body.

In some people with Dent disease, low levels of vitamin D and other factors can cause bones to soften and weaken. This can result in a condition called rickets or a similar condition called osteomalacia. These conditions can cause bone pain and make bones more likely to break. Rickets can also be associated with bowed legs, difficulty walking, and short stature.

Researchers have described two forms of Dent disease that are caused by changes in different genes: Dent disease 1 and Dent disease 2. Both forms are characterized by the features described above, but Dent disease 2 can also be associated with mild intellectual disabilities and developmental delays. People with Dent disease 2 may also have a clouding of the lens of the eye (cataract) that does not typically cause severe visual impairment. Studies have also suggested that people with Dent disease 2 may be more likely to develop a painful skin condition called hidradenitis suppurativa.

Frequency

Approximately 850 families with Dent disease have been reported in the scientific literature. However, because the features of Dent disease can vary and may overlap with those seen in other disorders, this number may not accurately represent the number of people with this condition.

Causes

Changes in the CLCN5 gene cause Dent disease 1, while changes in the OCRL gene cause Dent disease 2. Genetic changes that cause disease are called pathogenic variants. Approximately 60 percent of people with Dent disease have type 1. Another 15 to 20 percent of people with Dent disease have type 2.

The proteins produced from the CLCN5 and OCRL genes play important roles in normal kidney function, particularly within the proximal tubules. Studies suggest that certain pathogenic variants in the CLCN5 or OCRL genes lead to abnormal protein reabsorption within the proximal tubules. As a result, proteins that should be reabsorbed into the bloodstream are released in the urine. This leads to the kidney problems seen in people with Dent disease.

Approximately 20 to 25 percent of people with Dent disease do not have an identified variant in the CLCN5 or OCRL genes. The cause of the condition in these cases is not known.

Learn more about the genes associated with Dent disease

Inheritance

Dent disease is inherited in an X-linked pattern. The CLCN5 and OCRL genes are located on the X chromosome, which is one of the two sex chromosomes in each cell. In males (who have only one X chromosome), a pathogenic variant in the only copy of the gene in each cell is typically sufficient to cause the condition. This is not always the case for X-linked disorders in females (who have two X chromosomes in each cell). However, some females with a pathogenic variant in the CLCN5 or OCRL gene have mild features of Dent disease, including LMW proteinuria, hypercalciuria, and nephrolithiasis. Kidney failure in females is extremely rare. A characteristic of X-linked inheritance is that fathers cannot pass X-linked traits to their sons.

Some cases of Dent disease likely result from a new (de novo) variant in the gene that occurs during the formation of reproductive cells (eggs or sperm) in an affected individual's parent or during early embryonic development. These affected individuals typically have no history of the disorder in their family.

Other Names for This Condition

  • Dent syndrome
  • Dent's disease
  • Dents disease
  • Low-molecular-weight proteinuria with hypercalciuria and nephrocalcinosis
  • Renal Fanconi syndrome with nephrocalcinosis and renal stones
  • X-linked recessive hypercalciuric hypophosphatemic rickets
  • X-linked recessive nephrolithiasis

Additional Information & Resources

Genetic Testing Information

Genetic and Rare Diseases Information Center

Patient Support and Advocacy Resources

Clinical Trials

Catalog of Genes and Diseases from OMIM

Scientific Articles on PubMed

References

  • Bokenkamp A, Ariceta G, Bockenhauer D, Devuyst O, Emma F, van Bennekom D, Levtchenko E, Sayer J, Servais A, Vargas R, Zaniew M, Prikhodina L. Dent disease: clinical practice recommendations. Nephrol Dial Transplant. 2025 Apr 28;40(5):852-864. doi: 10.1093/ndt/gfaf003. Citation on PubMed
  • Claverie-Martin F, Ramos-Trujillo E, Garcia-Nieto V. Dent's disease: clinical features and molecular basis. Pediatr Nephrol. 2011 May;26(5):693-704. doi: 10.1007/s00467-010-1657-0. Epub 2010 Oct 10. Citation on PubMed
  • Devuyst O, Thakker RV. Dent's disease. Orphanet J Rare Dis. 2010 Oct 14;5:28. doi: 10.1186/1750-1172-5-28. Citation on PubMed or Free article on PubMed Central
  • Devuyst O. Dent's disease: chloride-proton exchange controls proximal tubule endocytosis. Nephrol Dial Transplant. 2010 Dec;25(12):3832-5. doi: 10.1093/ndt/gfq556. Epub 2010 Sep 6. No abstract available. Citation on PubMed
  • Ehlayel AM, Copelovitch L. Update on Dent Disease. Pediatr Clin North Am. 2019 Feb;66(1):169-178. doi: 10.1016/j.pcl.2018.09.003. Citation on PubMed
  • Hichri H, Rendu J, Monnier N, Coutton C, Dorseuil O, Poussou RV, Baujat G, Blanchard A, Nobili F, Ranchin B, Remesy M, Salomon R, Satre V, Lunardi J. From Lowe syndrome to Dent disease: correlations between mutations of the OCRL1 gene and clinical and biochemical phenotypes. Hum Mutat. 2011 Apr;32(4):379-88. doi: 10.1002/humu.21391. Epub 2011 Mar 10. Citation on PubMed
  • Hoopes RR Jr, Shrimpton AE, Knohl SJ, Hueber P, Hoppe B, Matyus J, Simckes A, Tasic V, Toenshoff B, Suchy SF, Nussbaum RL, Scheinman SJ. Dent Disease with mutations in OCRL1. Am J Hum Genet. 2005 Feb;76(2):260-7. doi: 10.1086/427887. Epub 2004 Dec 30. Citation on PubMed or Free article on PubMed Central
  • Jin YY, Huang LM, Quan XF, Mao JH. Dent disease: classification, heterogeneity and diagnosis. World J Pediatr. 2021 Feb;17(1):52-57. doi: 10.1007/s12519-020-00357-1. Epub 2020 Apr 4. Citation on PubMed
  • Lieske JC, Milliner DS, Beara-Lasic L, Harris P, Cogal A, Abrash E. Dent Disease. 2012 Aug 9 [updated 2017 Dec 14]. In: Adam MP, Bick S, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews(R) [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2026. Available from http://www.ncbi.nlm.nih.gov/books/NBK99494/ Citation on PubMed
  • Lloyd SE, Gunther W, Pearce SH, Thomson A, Bianchi ML, Bosio M, Craig IW, Fisher SE, Scheinman SJ, Wrong O, Jentsch TJ, Thakker RV. Characterisation of renal chloride channel, CLCN5, mutations in hypercalciuric nephrolithiasis (kidney stones) disorders. Hum Mol Genet. 1997 Aug;6(8):1233-9. doi: 10.1093/hmg/6.8.1233. Citation on PubMed
  • Marzuillo P, Piccolo V, Mascolo M, Apicella A, Argenziano G, Della Vecchia N, Guarino S, Miraglia Del Giudice E, La Manna A. Patients affected by dent disease 2 could be predisposed to hidradenitis suppurativa. J Eur Acad Dermatol Venereol. 2018 Aug;32(8):e309-e311. doi: 10.1111/jdv.14860. Epub 2018 Mar 25. No abstract available. Citation on PubMed
  • Wrong OM, Norden AG, Feest TG. Dent's disease; a familial proximal renal tubular syndrome with low-molecular-weight proteinuria, hypercalciuria, nephrocalcinosis, metabolic bone disease, progressive renal failure and a marked male predominance. QJM. 1994 Aug;87(8):473-93. Citation on PubMed

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