Main
Sir,
Distichiasis arises from the aberrant differentiation of meibomian glands of the eyelid, resulting in the development of a few, or sometimes a second inner row, of ‘eyelashes’. It can cause symptoms of corneal irritation and may need treatment. Primary distichiasis is thought to be only found as part of lymphoedema–distichiasis (LD) syndrome, although some individuals may only have signs of distichiasis and some only lymphoedema (less than 5% in each case).1 Primary lymphoedema is an accumulation of interstitial fluid that occurs as a result of reduced lymph drainage.2 It is visible clinically as swelling of the affected part. We present a family with the condition, their genetic mutation, and discuss the ophthalmologist's role on encountering such a case.
Case report
A 28-year-old woman was seen in our eye clinic with symptomatic distichiasis. Severe irritation caused by aberrant eyelashes rubbing her corneae had made her seek treatment. Initially epilation and subsequently electrolysis of the offending eyelashes gave her relief. The remainder of the anterior and posterior segment examination was unremarkable. Interestingly, she was noted to have lymphoedema of both lower extremities (Figure 1). Physical examination revealed no other abnormalities.
Family history
Her two sons, aged 8 and 4 years, were also found to have distichiasis but both were asymptomatic (Figure 2). Their physical examinations were unremarkable with no lymphoedema. She had three brothers (two of them twins) with distichiasis, and a sister with distichiasis as well as lymphoedema. In addition, she had two unaffected siblings. As none of the unaffected siblings would subject themselves to examination and investigation, their genotype could not be ascertained. A mutation in the FOXC2 gene was identified in the proband and shown to be inherited in both of her affected male offspring. This was a previously unpublished mutation, a 19 bp duplication: nt922-923insGCGCTGCCCTACGCCGCCG.
Discussion
Congenital distichiasis may result when a primary epithelial germ cell destined to differentiate into a specialised sebaceous gland (meibomian gland) of the tarsus develops into a complete pilosebaceous unit. The condition is frequently inherited in an autosomal dominant pattern with high penetrance but variable expressivity. During infancy, these fine, misdirected cilia are usually well tolerated despite their apposition to the globe. Clinical presentation may be delayed until the age of 5 years, when patients may complain of chronic ocular irritation.
Acquired distichiasis, on the other hand, occurs in the setting of chronic inflammation, especially in cicatricial conditions like ocular pemphigoid, Stevens–Johnson syndrome and following chemical injuries of the eyelid. Unlike congenital distichiasis, the cilia of acquired distichiasis tend to be nonpigmented and stunted and are more likely to cause symptomatic ocular irritation. The two varieties are differentiated relatively easily.
LD syndrome is an autosomal dominant disorder that classically presents as lymphoedema of the lower limbs (age of onset variable, but most often after puberty)3 and aberrant eyelashes. Ocular associations reported with distichiasis are: corneal hypoaesthesia;4 photophobia, ptosis, congenital ectropion and entropion, congenital cataracts, exotropia;3 absent lacrimal duct;5 epicanthus, telecanthus, blepharophimosis, colour blindness, eyelid oedema;6 microphthalmos, dystrophic retinal pigmentation and optic disc pallor as in the oculo-cerebro-renal syndrome.7
Other features described include synophrys (meeting of the eyebrows in the midline), venous abnormalities;8 congenital heart defects;3 cleft palate;6 spinal tumours9 and ectrodactyly.10 More recently, generalised or localised iris abnormalities, small corneal diameter and opacities as well as optic nerve hypoplasia have been noted.11 None of these features were present in our family, although only a limited slit-lamp assessment was possible in the boys because of their age.
The clinical diagnosis of lymphoedema is not always straightforward except in advanced cases where classical skin changes and brawny swelling become obvious. The confirmatory investigation is lymphoscintigraphy but false negatives can occur,8 as can age-related false positives. In the report by Brice et al,12 males had an earlier onset of lymphoedema and a significantly increased risk of complications. The gene for LD, located on the long arm of chromosome 16, is that encoding FOXC2, a forkhead family transcription factor involved in numerous developmental pathways.13 In all three members of the family presented in this report, a 19 bp insertion in the FOXC2 gene was identified. To our knowledge this mutation has not been previously reported.
Distichiasis is the most consistently inherited feature of LD syndrome. Lymphoedema in this condition is highly penetrant; however, it is rarely recognised before puberty. While examining young children with distichiasis, the likelihood of them developing lymphoedema subsequently should be borne in mind and parents counselled accordingly. As there are many interesting and unanswered questions regarding the connection between various associated features in LD, further research may give us the answers. Every ophthalmologist, on recognising a case of distichiasis should take a clear family history asking about lymphoedema of the lower limbs and the other features listed above, and arrange molecular genetic investigations to look for mutations in the FOXC2 gene. The family should also be referred for genetic counselling as there can be associated cleft palate and/or congenital heart disease. Any families where distichiasis but no lymphoedema occur are also of great interest, as it is not clear whether mutations in the FOXC2 gene would account for this symptom alone.
References
Jeffrey S . How double eyelashes give you swollen legs. Br J Ophthalmol 2002; 86: 1074.
Witte MH . Genetic alterations in lymphedema. Lymphology 1997; 16: 19–25.
Erickson RP, Dagenais SL, Caulder MS, Downs CA, Herman G, Jones MC et al. Clinical heterogeneity in lymphoedema-distichiasis with FOXC2 truncating mutations. J Med Genet 2001; 38(11): 761–766.
Kremer I, Weiberger D, Cohen S, Ben Sira I . Corneal hypoesthesia in asymptomatic familial distichiasis. Br J Ophthalmol 1986; 70(2): 132–134.
Holder-Espinasse M, de Bluis MC, Faivrel L, Romana S, Uteza Y, Munnich A et al. Absent lacrimal ducts, distichiasis, dysmorphic features and brachydactyly: a case report. Clin Dysmorphol 2001; 10(4): 253–255.
O’Donnell BA, Collin JR . Distichiasis: Management with cryotherapy to the posterior lamella. Br J Ophthalmol 1993; 77(5): 289–292.
Brancato R, Matteini M, Cotrozzi G . Sindrome oculo-cerebro-renale in soggott portare di blefarophimosi e di distichiasis. Ann Ottal 1965; 91: 35–37.
Rosbotham JL, Brice GW, Child AH, Nunan TO, Mortimer PS, Burnand KG . Distichiasis–lymphoedema: clinical features, venous function & lymphoscintigraphy. Br J Dermatol 2000; 142: 148–152.
Schwartz JF, O’Brien MS, Hoffman Jr JC . Hereditary spinal cysts, distichiasis and lymphedema. Ann Neurol 1980; 7: 340–343.
Lehmann OJ, Tuft S, Brice G, Smith R, Blixt A, Bell R et al. Novel anterior segment phenotypes resulting from forkhead gene alterations: evidence for cross-species conservation of function. Invest Ophthalmol Vis Sci 2003; 44: 2627–2633.
Collier MM . Ecrodactylie droite et distichiasis inferieur bilateral. Bull Soc D’Ophthalmol 1964; 64: 49–52.
Brice G, Mansour S, Bell R, Collin JR, Child AH, Brady AF et al. Analysis of the phenotypic abnormalities in lymphoedema–distichiasis syndrome in 74 patients with FOXC2 mutations or linkage to 16q24. J Med Genet 2002; 39(7): 478–483.
Fang J, Dagenais SL, Erickson RP, Arlt MF, Glynn MW, Gorski JL et al. Mutations in FOXC2 (MFH-1), forkhead family transcription factor, are responsible for the hereditary lyphedema–distichiasis syndrome. Am J Hum Genet 2000; 67: 1382–1388.
Acknowledgements
P Mortimer, AH Child and S Mansour, along with RB, GB and SJ, are all part of the Lymphoedema Research Group at St George's Hospital Medical School, collaborating with M Sarfarazi, University of Connecticut Health Centre USA, which enables the lymphoedema research programme to continue. RB was funded by the British Heart Foundation. The genetic analysis was carried out within the network of the London IDEAS Genetic Knowledge Park.
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Patil, B., Bell, R., Brice, G. et al. Distichiasis without lymphoedema?. Eye 18, 1270–1272 (2004). https://doi.org/10.1038/sj.eye.6701387
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DOI: https://doi.org/10.1038/sj.eye.6701387
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