Blount's disease
Blount's disease | |
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Other names | Tibia vara |
Blount's disease is inherited in an autosomal recessive manner (may be multifactorial as well).[1] | |
Specialty | Rheumatology |
Blount's disease (or Blount disease) is a growth disorder of the
Signs and symptoms
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Cause
Blount disease is a growth disorder of the
Diagnosis
Differential diagnosis
Lower extremity deformities in
Treatment
Children who develop severe bowing before the age of 3 may be treated with knee ankle foot orthoses.[9] However, bracing may fail, or bowing may not be detected until the child is older. Bracing should be started by 3 years of age. In some cases, surgery may be performed.[10][2][11][8]
Blount disease is one of the 8 severe comorbidities of
Etymology
Blount disease is named after Walter Putnam Blount (1900–1992), an American pediatric orthopedic surgeon, who described it in 1937.[13][14] It has also been known as Mau-Nilsonne syndrome, after C. Mau and H. Nilsonne, who published early case reports of the condition.[15][16] it is today considered an acquired disease of the proximal tibial metaphysis rather than an epiphyseal dysplasia or osteochondrosis.[11]
References
- ^ "OMIM Entry 259200 - BLOUNT DISEASE, ADOLESCENT". omim.org. Retrieved 7 November 2017.
- ^ ISBN 0-07-143833-5.
- S2CID 31733527.
- ^ Dakshina Murthy T S. S; Alessandro De Leucio. Blount Disease Treasure Island (FL): StatPearls Publishing; 2022 January.
- PMID 32159063.
- S2CID 79825711.
- ]
- ^ ISSN 2076-3417.
- S2CID 24907234.
- S2CID 21625248.
- ^ ISBN 978-0-323-07243-4.
- S2CID 204947687.
- Who Named It?
- ^ W. P. Blount. Tibia vara: osteochondrosis deformans tibiae. Journal of Bone and Joint Surgery, Boston, 1937, 19: 1-29.
- ^ Mau, C. (1923/24) Genu varum bedingt durch Tihiaepiphysendefekt bei Kartilaginärer Exostose. Z. orthop. Chir. 44, 383.
- ^ Nilsonne, H. (1929) Genu varum mit eigentümlichen Epiphysenveränderungen. Acta chir. scand. 44, 187.
External links
- Dakshina Murthy T S. S; Alessandro De Leucio. Blount Disease Treasure Island (FL): StatPearls Publishing; 2022 Jan-.