Wikipedia

Brachydactyly

(Redirected from Osebold Remondini syndrome)

Brachydactyly (from Greek βραχύς (brachus) 'short' and δάκτυλος (daktulos) 'finger') is a medical term denoting the presence of abnormally short digits (fingers or toes) at birth. The shortness is relative to the length of other long bones and other parts of the body. Brachydactyly is an inherited, dominant trait. It most often occurs as an isolated dysmelia, but can also occur with other anomalies as part of many congenital syndromes. Brachydactyly may also be a signal that one is at risk for congenital heart disease[1] due to the association between congenital heart disease and Carpenter syndrome and the link between Carpenter syndrome and brachydactyly.[2]

Brachydactyly
Different forms of brachydactyly
SpecialtyMedical genetics Edit this on Wikidata

Nomograms for normal values of finger length as a ratio to other body measurements have been published. In clinical genetics, the most commonly used index of digit length is the dimensionless ratio of the length of the third (middle) finger to the hand length. Both are expressed in the same units (centimeters, for example) and are measured in an open hand from the fingertip to the principal creases where the finger joins the palm and where the palm joins the wrist.

Causes

edit

Generally, brachydactyly is inherited through an autosomal dominant trait (The exact gene may differ see "Types" table for specific genes). However exceptions could exist due to antiepileptic medicines taken during pregnancy[3] or low blood flow to the extremities during infancy.[4]

Symptoms

edit

Symptoms of isolated brachydactyly include shorter bones in the hands and feet. This could include, phalanges, metacarpals, metatarsals, carpals, and tarsals. Different types of isolated brachydactyly have different symptoms and they are grouped according to what areas they affect.

Prognosis

edit

Isolated brachydactyly does not affect the wellbeing nor longevity of one's life, in most cases treatment is not necessary.[4] The trait is primarily a cosmetic one and does not, in most cases, affect function of the hands and feet. Even left untreated and affecting function the general diagnosis of brachydactyly does not impact life expectancy. Prognosis may differ with different types or syndromes. ie. brachydactyly-mesomelia-intellectual disability-heart defects syndrome or if brachydactyly is not isolated and is a part of a larger genetic condition. In rare cases of isolated untreated brachydactyly, simple functions like walking or grabbing objects may be difficult, reducing the overall quality of life.

Treatment

edit

Treatment is only needed if brachydactyly affects the function of the phalanges. In rare cases where function is affected, reconstructive surgery is used to improve function and the ability to use one's phalanges. Another treatment includes cosmetic surgery (which is often confused with reconstructive surgery but differs in that cosmetic surgery may not be seen as medically necessary while reconstructive is) to change the way the affected areas appear.[4]

Diagnosis

edit

Brachydactyly is usually diagnosed through anthropometric, clinical, or radiological methods. It is usually found early during infancy or in childhood years when the size difference becomes noticeable. It normally gets diagnosed as the difference in phalange size becomes more apparent. Healthcare providers complete a medical history, physical exam of symptoms and use radiographs (X-rays). The X-rays show whether certain bones are shorter than others or shorter than they are in expected to be. Along with these diagnostic steps the healthcare provider may conduct a genetic test. This could be to see if the disorder runs in the family and has been passed down or to identify the defective gene.

Epidemiology

edit

Most isolated forms of brachydactyly are considered rare, that is, diseases affecting less 200,000 people.[5] However, type A3 and type D are relatively common, affecting around 2% of the population.[6] Particularly high prevalence of brachydactyly type D was reported among Israeli Arabs and in the Japanese population.[7] Type A3 was found at an especially high frequency of 21% among Japanese schoolchildren.[8]

Types

edit

There are several types of brachydactyly:

Type OMIM Gene Locus Also known as Description
Type A1, BDA1 112500 IHH BDA1B 5p13.3-p13.2, 2q33-q35 Brachydactyly type A1 or Farabee-type brachydactyly. BDA1 is an autosomal dominant inherited disease. Features include: short or absent phalanges, extra carpal bones, hypoplastic or absent ulna and short metacarpal bones.
Type A2, BDA2 112600 BMPR1B GDF5 20q11.2, 4q23-q24 Brachydactyly type A2, Brachymesophalangy II or Brachydactyly Mohr-Wriedt type. Type A2 is a very rare form of brachydactyly. The phalanges of the index fingers and second toes are shortened.[9]
Type A3, BDA3 112700 HOXD13 Brachydactyly type A3, brachymesophalangy V or brachydactyly-clinodactyly. Type A3 only shortens the middle bone of the little finger.[9]
Type A4, BDA4 112800 HOXD13 2q31-q32 Brachydactyly type A4, brachymesophalangy II and V or brachydactyly temtamy type. Characterized by shortened 2nd and 5th fingers and an absence of the 2nd-5th lateral toes.[9]
Type A5, BDA5 112900 Brachydactyly type A5 nail dysplasia.
Type A6, BDA6 112910 Brachydactyly type A6 or Osebold-Remondini syndrome.
Type A7, BDA7 Brachydactyly type A7 or brachydactyly smorgasbord type.[10]
Type B, BDB (or BDB1) 113000 ROR2 9q22 Brachydactyly type B or Cooks syndrome. Type B affects the final bones of all eight fingers. It causes the bone to be shortened or missing entirely. The same thing happens to the corresponding toes. The final thumb bones and big toe bones may be split or flatter than average.[9]
Type C, BDC 113100 GDF5 20q11.2 Brachydactyly type C or Brachydactyly Haws type. This rare form of brachydactyly only affects three fingers on each hand. The index, middle, and little finger will have their middle bone shortened. The ring finger will not be affected. As a result, type C brachydactyly will leave the ring finger as the longest on the hand.[9]
Type D, BDD 113200 HOXD13 2q31-q32 Brachydactyly type D. "Stub Thumb" Referred to inaccurately as "clubbed thumbs".[11] Most common form of brachydactyly. It shortens the final bone in the thumbs and does not affect the fingers at all.[9]
Type E, BDE 113300 HOXD13 2q31-q32 Brachydactyly type E. This is the rarest form of brachydactyly. It is most often part of another condition that someone is born with. Type E shortens the bones in the hands and feet along with the bottom bone in the fingers. Instead of making the fingers and toes look shorter, it makes the hands and feet look smaller.[9]
Type B and E 112440 ROR2 HOXD13 9q22, 2q31-q32 Brachydactyly types B and E combined, Ballard syndrome or Pitt-Williams brachydactyly.
Type A1B, BDA1B 607004 5p13.3-p13.2 Brachydactyly type A1, B.

Other syndromes

edit

In the above brachydactyly syndromes, short digits are the most prominent of the anomalies, but in many other syndromes (Down syndrome, Rubinstein–Taybi syndrome, etc.), brachydactyly is a minor feature compared to the other anomalies or problems comprising the syndrome.

See also

edit

References

edit
  1. ^ Pierpont, Mary Ella; Brueckner, Martina; Chung, Wendy K.; Garg, Vidu; Lacro, Ronald V.; McGuire, Amy L.; Mital, Seema; Priest, James R.; Pu, William T.; Roberts, Amy; Ware, Stephanie M.; Gelb, Bruce D.; Russell, Mark W. (2018-11-20). "Genetic Basis for Congenital Heart Disease: Revisited". Circulation. 138 (21): e653–e711. doi:10.1161/CIR.0000000000000606. ISSN 0009-7322. PMC 6555769. PMID 30571578.
  2. ^ Jenkins, Dagan; Seelow, Dominik; Jehee, Fernanda S.; Perlyn, Chad A.; Alonso, Luís G.; Bueno, Daniela F.; Donnai, Dian; Josifiova, Dragana; Mathijssen, Irene M. J.; Morton, Jenny E. V.; Helene Ørstavik, Karen; Sweeney, Elizabeth; Wall, Steven A.; Marsh, Jeffrey L.; Nürnberg, Peter (2007-06-01). "RAB23 Mutations in Carpenter Syndrome Imply an Unexpected Role for Hedgehog Signaling in Cranial-Suture Development and Obesity". The American Journal of Human Genetics. 80 (6): 1162–1170. doi:10.1086/518047. ISSN 0002-9297. PMC 1867103. PMID 17503333.
  3. ^ Wlodarczyk, Bogdan J.; Palacios, Ana M.; George, Timothy M.; Finnell, Richard H. (2012). "Antiepileptic drugs and pregnancy outcomes". American Journal of Medical Genetics Part A. 158A (8): 2071–2090. doi:10.1002/ajmg.a.35438. PMC 3402584. PMID 22711424.
  4. ^ a b c "Brachydactyly Types - Causes & Outlook". Cleveland Clinic. Archived from the original on 2022-10-13. Retrieved 2022-10-13.
  5. ^ "Rare Diseases FAQ". Genome.gov. Archived from the original on 2022-10-13. Retrieved 2022-10-13.
  6. ^ Temtamy, Samia A.; Aglan, Mona S. (2008-06-13). "Brachydactyly". Orphanet Journal of Rare Diseases. 3 (1): 15. doi:10.1186/1750-1172-3-15. ISSN 1750-1172. PMC 2441618. PMID 18554391.
  7. ^ Temtamy, Samia (1978). ""The genetics of hand malformations."". Birth Defects Original Article Series. 14 (3): i–xviii, 1–619. PMID 215242.
  8. ^ Idengaku Zasshi, Jinrui (1962) [March 1962]. "The Japanese journal of human genetics". The Japanese Journal of Human Genetics. 7: 10–9. ISSN 0021-5074.
  9. ^ a b c d e f g Brennan, Dan. "What Is Brachydactyly?". WebMD. Archived from the original on 2022-10-13. Retrieved 2022-10-13.
  10. ^ Meiselman SA, Berkenstadt M, Ben-Ami T, Goodman RM (1989). "Brachydactyly type A-7 (Smorgasbord): a new entity". Clin. Genet. 35 (4): 261–7. doi:10.1111/j.1399-0004.1989.tb02940.x. PMID 2714013. S2CID 30099363.
  11. ^ "Clubbing of the Nails: Background, Pathophysiology, Epidemiology". 15 July 2021. Archived from the original on 20 November 2021. Retrieved 18 September 2015.
edit
Retrieved from "https://en.wikipedia.org/w/index.php?title=Brachydactyly&oldid=1253810118"