Weismann-Netter-Stuhl syndrome

Weismann-Netter-Stuhl syndrome is inherited in an autosomal dominant manner

Weismann-Netter-Stuhl syndrome, also known as Weismann-Netter Syndrome or more technically by the term tibioperoneal diaphyseal toxopachyosteosis, is a rare disorder characterized by bowing of the lower legs and an abnormal thickening of thinner bone in the leg.[1]

The main sign is anterior bowing and posterior cortical thickening of the diaphyses of both the tibiae and fibulae. It is thought to be inherited in an autosomal dominant fashion, and is most often bilateral and symmetric in nature. Associated features include dwarfism and mild intellectual disability, as well as a process known as tibialization of the fibulae, which involves thickening and enlargement of these bones to an extent resembling the tibiae.[2] The combination of the presence of tibialization of the fibulae, which is highly specific for the disorder, and the absence of laboratory abnormalities ruling out alternative diagnoses including rickets, essentially confirms the diagnosis.

## Contents

* 1 Cause
* 2 Diagnosis
* 2.1 Radiographic features
* 3 Management
* 4 History
* 5 References
* 6 External links

## Cause

## Diagnosis

### Radiographic features

The most prominent and extensively documented findings of Weismann-Netter-Stuhl syndrome are on plain radiographs of the bones. Findings include bilateral and symmetric anterior bowing of both tibiae and fibulae, lateral bowing of the tibiae, femoral bowing, and squaring of iliac and pelvis bones.[3]

## Management

## History

French doctors Weismann-Netter and Stuhl characterized the features of this disorder in their report first describing the association in seven patients in 1954.[4] They believed these seven patients had mistakenly been diagnosed as congenital syphilis or rickets, which remain the primary considerations in the differential diagnosis of this syndrome today.

## References

1. ↑ Gupta, P.; Mittal, R.; Mittal, S.; Shankar, V. (2014). "Weismann-Netter-Stuhl syndrome: report of two cases and treatment". Case Reports 2014 (feb04 2): bcr2013201772–bcr2013201772. doi:10.1136/bcr-2013-201772. ISSN 1757-790X.
2. ↑ Robinow M, Johnson GF. The Weismann-Netter syndrome. Am J Med Genet. 1988 Mar;29(3):573-9. PubMed PMID 3377000.
3. ↑ Peippo, M., Valanne, L., Perhomaa, M., Toivanen, L., Ignatius, J. Weismann-Netter syndrome and mental retardation: a new patient and review of the literature. Am. J. Med. Genet. 149A: 2593-2601, 2009. [PubMed: 19839038]
4. ↑ Weismann-Netter, R., Stuhl, L. D'une osteopathie congenitale eventuellement familiale. Presse Med. 62: 1618-1622, 1954. [PubMed: 13237064].

## External links

Classification|

* ICD-10: Q77.8
* OMIM: 112350

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External resources|

* Orphanet: 3344

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