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Yellow Nail Syndrome

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421. Yellow Nail Syndrome

issue with this page, please visit our . Thank you, we just sent a survey email to confirm your preferences. Further reading and references ; Nail disorders and systemic disease: what the nails tell us. J Fam Pract. 2008 Aug57(8):509-14. ; Yellow nail syndrome. Curr Opin Pulm Med. 2009 Jul15(4):371-5. doi: 10.1097/MCP.0b013e32832ad45a. ; Yellow nail syndrome: analysis of 41 consecutive patients. Chest. 2008 Aug134(2):375-81. doi: 10.1378/chest.08-0137. Epub 2008 Apr 10. ; DermNet NZ ; Yellow nail (...) Guidelines. You may find the article more useful, or one of our other . In this article In This Article Yellow Nail Syndrome In this article Yellow nail syndrome (YNS) is a rare disorder, in which there is a triad of: Nail discolouration and nail dystrophy. Lymphoedema. Chronic respiratory disorders It was first described by Samman in 1964. Epidemiology It is very rare with only around 150 published cases. [ ] Men and women are equally affected. [ , ] Aetiology [ , ] Both familial and sporadic cases have

2008 Mentor

422. Dietary treatment of chylous ascites in yellow nail syndrome. Full Text available with Trip Pro

Dietary treatment of chylous ascites in yellow nail syndrome. Chylous ascites has rarely been reported in yellow nail syndrome. A case of chylous ascites in yellow nail syndrome is described which was treated successfully with dietary restriction of fat and supplements of medium chained triglycerides.

1989 Gut

423. Chylous ascites, intestinal lymphangiectasia and the 'yellow-nail' syndrome. Full Text available with Trip Pro

in most individuals revealed hypoplasia, or aplasia of the lymphatics, similar to that occurring in primary lymphoedema: other patients also developed pleural effusions of high protein content or ascites suggestive of a more generalised disorder of the lymphatic system. Here we describe a patient in whom the classical 'yellow-nail' syndrome was associated with intestinal and chylous ascites. (...) Chylous ascites, intestinal lymphangiectasia and the 'yellow-nail' syndrome. In 1964 Samman and White described 13 patients with lymphoedema of the lower extremities associated with an unusual dystrophy of the finger and toe nails: this they termed the 'yellow-nail' syndrome. Affected nails were thickened, excessively curved along both axes, very slow growing and of yellowish-grey hue; cuticle and lunula were usually absent and onycholysis was frequently evident. Lower limb lymphangiography

1985 Gut

424. Conjunctival changes associated with yellow nail syndrome Full Text available with Trip Pro

Conjunctival changes associated with yellow nail syndrome 12140219 2002 09 26 2018 11 13 0007-1161 86 8 2002 Aug The British journal of ophthalmology Br J Ophthalmol Conjunctival changes associated with yellow nail syndrome. 930 Bourcier T T Baudrimont M M Borderie V V Mayaud C C Laroche L L eng Case Reports Letter England Br J Ophthalmol 0421041 0007-1161 IM Bronchiectasis complications Conjunctival Diseases complications Humans Male Maxillary Sinusitis complications Middle Aged Nail Diseases (...) complications Syndrome 2002 7 26 10 0 2002 9 27 6 0 2002 7 26 10 0 ppublish 12140219 PMC1771239 J Am Acad Dermatol. 1990 Apr;22(4):608-11 2319021 Br J Dermatol. 1964 Apr;76:153-7 14140738 Postgrad Med J. 1997 Aug;73(862):466-8 9307736 Br J Dermatol. 1996 Feb;134(2):307-12 8746347

2002 The British journal of ophthalmology

425. Coexistent yellow nail syndrome and selective antibody deficiency. (Abstract)

Coexistent yellow nail syndrome and selective antibody deficiency. Yellow nail syndrome (YNS) is a rare, often underdiagnosed condition of unknown origin. The clinical features of the syndrome include yellow nails, chronic sinusitis, bronchiectasis, pleural effusion, and lymphoedema. Despite the frequent occurrence of upper and lower respiratory tract infections in patients with YNS, comprehensive analysis of their humoral immunity has not been previously reported.To present the case (...) of a patient with YNS whose recurrent upper and lower respiratory tract infections may have been caused by an underlying selective antibody deficiency that manifests as impaired IgG antibody response to polysaccharide antigens.The patient underwent cultures of purulent sputum for Streptococcus pneumoniae and Haemophilus influenzae, bronchial washings for H. influenzae, and nail scrapings for fungi. Her serum levels of IgG, IgA, IgM, IgG subclasses, and serum titers of IgG antitetanus toxoid, anti-H

2003 Asthma & Immunology

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