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Laurence-Moon Syndrome

Known as: Laurence-Moon Syndrome [Disease/Finding], Syndrome, Laurence-Moon-Biedl, biedl lawrence moon syndrome 
A rare genetic syndrome with an autosomal recessive pattern of inheritance. Mutations in the BBS5 and MKKS genes of chromosome 11 have been observed… 
National Institutes of Health

Related topics

Related topics

16 relations
AtaxiaAutosomal recessive inheritanceBardet-Biedl SyndromeCongenital hypoplasia of penis

Broader (1)

Hereditary Diseases

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Combining user involvement with innovative design to develop a radical new method for managing N fertilization
In France, a single science-based model has dominated winter wheat N fertilizer management for 40 years. Despite scientific… 
2011
2011
Heteroskedasticity and Spatiotemporal Dependence Robust Inference for Linear Panel Models with Fixed Effects
This paper studies robust inference for linear panel models with fixed effects in the presence of heteroskedasticity and… 
Highly Cited
2009
Highly Cited
2009
Feasibility of recommending certain replacement or alternative fats
Expert groups and public health authorities recommend that trans-fatty acid (TFA) intakes from industrially produced partially… 
1997
1997
Renal involvement in the Laurence-Moon-Bardet-Biedl syndrome: report of five cases
Abstract.We report five patients with Laurence-Moon-Bardet-Biedl syndrome (LMBBS) who had renal involvement. Intravenous… 
Highly Cited
1996
Highly Cited
1996
Revision of Pearcea (Gesneriaceae)
Kvist, Lars Peter, and Laurence E. Skog. Revision of Pearcea (Gesneriaceae). Smithsonian Contributions to Botany, number 84,47… 
1986
1986
Retinal and neurologic findings in the Laurence-Moon-Bardet-Biedl phenotype.
Highly Cited
1986
Highly Cited
1986
Laurence Sterne, the later years
Laurence Sterne, humorist, sentimentalist and Anglican divine, is recognized as one of the greatest English novelists, though he… 
1973
1973
Urographic findings in the Bardet-Biedl syndrome, formerly the Laurence-Moon-Biedl syndrome.
Six cases of Bardet-Biedl syndrome are presented. Common findings in this syndrome include mental retardation, pigmentary… 
1967
1967
Hereditary syndromes with auditory and dermatological manifestations.
Congenital deafness may be associated with hereditary disorders of keratinization. Pili torti, twisted hair, was first reported… 
Highly Cited
1943
Highly Cited
1943
Further Consideration of the Cushing Syndrome1
FOR several years we have endeavored to follow the reported cases of the Cushing syndrome. In many instances, by correspondence… 
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