Kirner's deformity, also known as dystelephangy, is an uncommon genetic hand malformation which is characterized by a radial and volar curvature of the distal phalange of the fifth (pinky) finger. It is merely cosmetic and doesn't affect hand function.[2]
Kirner's deformity | |
---|---|
Other names | Dystelephangy, Congenital bilateral metadiaphyseal acrodysplasia of the little finger[1] |
This trait is often hereditary, and is thought to be inherited in an autosomal dominant manner with reduced penetrance | |
Specialty | Medical genetics |
Symptoms | Radial and volar curvature of the distal phalange of the fifth finger. |
Complications | None |
Types | There are congenital, early-onset, and acquired forms. |
Causes | Autosomal dominant inheritance |
Prevention | None |
Treatment | Usually, none is required, surgery is done due to cosmetic reasons |
Prognosis | Good |
Frequency | Uncommon, about 1 in 400-600 people are thought to have this deformity |
Deaths | Deaths are not involved with the deformity, since it isn't deadly. |
Etymology
editThis condition is considered to be a type of isolated brachydactyly.[3]
A.R. Thomas et al. described it as a "dystrophy of the fifth finger".[4]
History
editThis difference was first discovered in 1927 by Kirner et al., when he described a 13-year-old girl with the characteristic radial and volar curvature of the fifth finger's distal phalanx bone.[5]
Signs and symptoms
editThis anomaly is characterized by the painless curvature and "bulbing" of the distal end of the little finger.[6] The time of onset varies among people, but the two most common ages of onset are birth and adolescence, although there can be cases where one is already born with a Kirner's deformity that worsens as one grows older (progressive).[7]
Rarely, multiple fingers (which may or may not include the little finger) may be affected with Kirner's deformity; this is known as polytopic dystelephalangy, and cases like this typically have a strong genetic link.[8]
Other isolated congenital deformities of the hand can occur alongside this deformity; one such instance is the family described by Erduran et al., which presented both camptodactyly and Kirner's deformity.[9]
Radiological findings
editThe following list comprises the radiological findings associated with Kirner's deformity that have been described in medical literature:[7][10][11]
- Diaphyseal shortening
- Diaphyseal curvature
- Epiphyseal curvature
- Sclerosing of the diaphyses
- Agenesis of the little finger's flexor digitorum superficialis tendon.
- Abnormal cartilage placement of the diaphyses and the flexor tendon
- Radiolucent nidus in the little finger's distal tuft.
- L-shaped physis
Causes
editThis deformity is caused by a widening of the epiphyseal plate of the fifth finger's distal phalange.[12] Another proposed cause involves the abnormal insertion of the flexor digitorum profundus in the volar area of the fifth finger's distal phalange.[13] It is thought to be an autosomal dominant trait with reduced penetrance.[14]
Diagnosis
editThis condition can be diagnosed by physical examination and radiographic imaging, including X-rays, magnetic resonance imaging, etc.[citation needed]
Differential diagnosis
editThis condition can be confused with other malformations (congenital and acquired) of the hand, these include:
- Camptodactyly[15][16]
- Clinodactyly[17][16]
- Mallet finger[18]
- Fracture[19]
- Brachydactyly type A3 (also known as brachymesophalangy type V)[20]
Epidemiology
editThis hand difference is estimated to be present in 0.15%-0.25% of the world population.[21]
It is more common in women than in men;[12] physical examination performed on people from a selected region in southern England by David and Burwood et al. found 18 individuals from 9 families with Kirner's deformity. Of these 18 individuals, 6 were men and 12 were women.[22]
Treatment
editA handful of treatment methods resulting in successful improvement of Kirner's deformity have been described, these include:
Associations
editThe following subsections comprise Kirner deformity's non-syndromic and syndromic associations:[16][7][29]
Non-syndromic
editSyndromic
editThese are the syndromes associated with this malformation
See also
editReferences
edit- ^ "Dystelephalangy". 16 June 2022.
- ^ Gujjar, Rakesh; Khanna, Vikram; Kollu, Raja; Vaishya, Raju (2016-09-01). "Kirner's deformity – A case report". Apollo Medicine. 13 (3): 187–188. doi:10.1016/j.apme.2015.07.002.
- ^ Temtamy, Samia A; Aglan, Mona S (2008-06-13). "Brachydactyly". Orphanet Journal of Rare Diseases. 3: 15. doi:10.1186/1750-1172-3-15. PMC 2441618. PMID 18554391.
- ^ Thomas, A. R. (1936). "A New Dystrophy of the Fifth Finger". The Lancet. 228 (5890): 163–164. doi:10.1016/S0140-6736(00)81788-2. S2CID 196407714.
- ^ Rasmussen, Lars Bjørn (1981-01-01). "Kirner's Deformity: Juvenile Spontaneous Incurving of the Terminal Phalanx of the Fifth Finger". Acta Orthopaedica Scandinavica. 52 (1): 35–37. doi:10.3109/17453678108991755. PMID 7211313.
- ^ "Dystelephalangy - About the Disease - Genetic and Rare Diseases Information Center". rarediseases.info.nih.gov. Retrieved 2022-09-01.
- ^ a b c Sargent, Michael. "Kirner deformity | Radiology Reference Article | Radiopaedia.org". Radiopaedia. Retrieved 2022-09-01.
- ^ Sugiura, Y. (1989-07-01). "Polytopic dystelephalangy of the fingers". Pediatric Radiology. 19 (6): 493–495. doi:10.1007/BF02387670. PMID 2771501. S2CID 26382843.
- ^ Erduran, Mehmet; Altinisik, Julide; Meric, Gokhan; Ulusal, Ali Engin; Akseki, Devrim (2013). "Camptodactyly and Kirner's Deformity in one Family". Balıkesır Health Sciences Journal. 2 (1): 36–39. doi:10.5505/bsbd.2013.03522.
- ^ Satake, Hiroshi; Ogino, Toshihiko; Eto, Jun; Maruyama, Masahiro; Watanabe, Tadayoshi; Takagi, Michiaki (June 2013). "Radiographic features of Kirner's deformity". Congenital Anomalies. 53 (2): 78–82. doi:10.1111/cga.12010. PMID 23751041. S2CID 5379782.
- ^ Fairbank, S. M.; Rozen, W. M.; Coombs, C. J. (2014-09-30). "The pathogenesis of Kirner's deformity: A clinical, radiological and histological study". Journal of Hand Surgery (European Volume). 40 (6): 633–637. doi:10.1177/1753193414551911. PMID 25274771. S2CID 1811920.
- ^ a b Adeb, Melkamu; Hayashi, Daichi; Kumar, Yogesh (2016-10-21). "Kirner's deformity of the fifth finger: a case report". BMC Musculoskeletal Disorders. 17 (1): 440. doi:10.1186/s12891-016-1300-8. PMC 5073483. PMID 27769216.
- ^ Lee, Jaejoon; Ahn, Joong Kyong; Choi, Sang-Hee; Koh, Eun-Mi; Cha, Hoon-Suk (September 2010). "MRI findings in Kirner deformity: normal insertion of the flexor digitorum profundus tendon without soft-tissue enhancement". Pediatric Radiology. 40 (9): 1572–1575. doi:10.1007/s00247-010-1628-4. PMID 20336287. S2CID 29662827.
- ^ Tianxiao, Ma; Wang, Dongyue; Song, Lihua (2020-09-25). "Kirner's deformity of the fifth finger: A case report". Medicine. 99 (39): e22294. doi:10.1097/MD.0000000000022294. PMC 7523806. PMID 32991433.
- ^ Dubrana, F.; Dartoy, C.; Stindel, E.; Fenoll, B.; Le Nen, D.; Lefevre, C. (1995). "[Kirner's deformity. 4 case reports and review of the literature]". Annales de Chirurgie de la Main et du Membre Supérieur. 14 (1): 33–37. doi:10.1016/s0753-9053(05)80532-0. PMID 7535545.
- ^ a b c d e Viswanathan, Vijay; Mhapankar, Abhijit V. (2018). "Kirner's Syndrome: Displaced Bone – Misplaced Diagnosis" (PDF). Indian Pediatrics. 55 (7): 625–. doi:10.1007/s13312-018-1314-4. PMID 30129560. S2CID 52046544.
- ^ Dubrana, F.; Dartoy, C.; Stindel, E.; Fenoll, B.; Le Nen, D.; Lefevre, C. (1995). "[Kirner's deformity. 4 case reports and review of the literature]". Annales de Chirurgie de la Main et du Membre Supérieur. 14 (1): 33–37. doi:10.1016/s0753-9053(05)80532-0. PMID 7535545.
- ^ Walsh, Catherine; Sills, Matthew; Markey, Gerard (2018-11-01). "An 11-year-old with mallet finger". Emergency Medicine Journal. 35 (11): 679–680. doi:10.1136/emermed-2017-207361. PMID 30337418. S2CID 53013535.
- ^ Khalid, Saifullah; Khalid, Mohd; Zaheer, Samreen; Ahmad, Ibne; Ullah, Ekram (2012). "Kirner's Deformity Misdiagnosed as Fracture: A Case Report". Oman Medical Journal. 27 (3): 237–238. doi:10.5001/omj.2012.53. PMC 3394366. PMID 22811775.
- ^ "Entry - %128000 - DYSTELEPHALANGY - OMIM". omim.org. Retrieved 2022-09-02.
- ^ Tianxiao, Ma; Wang, Dongyue; Song, Lihua (2020-09-25). "Kirner's deformity of the fifth finger: A case report". Medicine. 99 (39): e22294. doi:10.1097/MD.0000000000022294. PMC 7523806. PMID 32991433.
- ^ David, T. J.; Burwood, R. L. (1972-12-01). "The nature and inheritance of Kirner's deformity". Journal of Medical Genetics. 9 (4): 430–433. doi:10.1136/jmg.9.4.430. PMC 1469067. PMID 4646550.
- ^ Khalid, Saifullah; Khalid, Mohd; Zaheer, Samreen; Ahmad, Ibne; Ullah, Ekram (May 2012). "Kirner's Deformity Misdiagnosed as Fracture: A Case Report". Oman Medical Journal. 27 (3): 237–238. doi:10.5001/omj.2012.53. PMC 3394366. PMID 22811775.
- ^ Mantero, R. (1982). "[Kirner's disease: surgical treatment]". Annales de Chirurgie de la Main. 1 (1): 88–91. doi:10.1016/s0753-9053(82)80049-5. PMID 9303047.
- ^ Freiberg, A.; Forrest, C. (January 1986). "Kirner's deformity: A review of the literature and case presentation". Journal of Hand Surgery. 11 (1): 28–32. doi:10.1016/S0363-5023(86)80095-8. PMID 3944436.
- ^ Gamo, Kazushige; Kuriyama, Kohji; Uesugi, Ayako; Nakase, Takanobu; Hamada, Masayuki; Kawai, Hideo (2014). "Percutaneous corrective osteotomy for Kirner's deformity". Journal of Pediatric Orthopaedics B. 23 (3): 277–281. doi:10.1097/BPB.0000000000000042. PMID 24590256.
- ^ a b c "Kirner deformity - General Practice notebook". gpnotebook.com. Retrieved 2022-09-01.
- ^ Horii, Emiko; Otsuka, Junko; Koh, Shukuki (2018-02-26). "Surgical Treatment for Kirner's Deformity—Single Osteotomy through a Palmar Approach". Plastic and Reconstructive Surgery Global Open. 6 (2): e1683. doi:10.1097/GOX.0000000000001683. PMC 5865914. PMID 29616176.
- ^ Lee, Fred A. (1968-12-01). "Generalized Overconstriction of Long Bones and Unilateral Kirner's Deformity in a deLange Dwarf". American Journal of Diseases of Children. 116 (6): 599–603. doi:10.1001/archpedi.1968.02100020603005. PMID 5697191.