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Year : 2005  |  Volume : 71  |  Issue : 3  |  Page : 186-188

Ehlers danlos syndrome in two siblings

1 Department of Dermatology, Venereology and Leprosy, JLN Hospital and Research Centre, Bhilai Steel Plant, Bhiali, India
2 Department of Medicine, JLN Hospital and Research Centre, Bhilai Steel Plant, Bhiali, India

Correspondence Address:
M N Das
4-A/41/7, Bhilai, Chattisgarh
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Source of Support: None, Conflict of Interest: None

DOI: 10.4103/0378-6323.16235

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Two cases of Ehlers-Danlos syndrome affecting two real brothers are being reported. Both of them presented with features of atrophy and hyperextensibility of skin, hypermobility of joints and scarring at the sites of trauma. The elder brother also had kyphoscoliosis and hypogonadism with testicular failure.

Keywords: Ehlers Danlos syndrome, Kyphoscoliosis, Hypogonadism

How to cite this article:
Das M N, Ghorpade A, Mercy P, Pandey T K, Sharma R. Ehlers danlos syndrome in two siblings. Indian J Dermatol Venereol Leprol 2005;71:186-8

How to cite this URL:
Das M N, Ghorpade A, Mercy P, Pandey T K, Sharma R. Ehlers danlos syndrome in two siblings. Indian J Dermatol Venereol Leprol [serial online] 2005 [cited 2021 Jan 21];71:186-8. Available from:

  Introduction Top

Ehlers-Danlos syndrome is a group of generalized disorders of connective tissue characterized by hyperextensibility of skin, hypermobility of joints and fragility of skin and blood vessels.[1] More than ten clinical types have been described on the basis of clinical, genetic and biochemical information.[2] The basic defect in this disease is abnormality in the biosynthesis of collagen. It may be inherited as an autosomal dominant, autosomal recessive or X- linked recessive trait.

  Case reports Top

A 15-year-old boy (Case 1) born out of a consanguineous marriage presented with repeated scarring over both the knee and elbow joints since infancy. He was referred to us to rule out leprosy. His elder brother (Case 2), aged 17, also had similar skin lesions.

Cutaneous examination of both the brothers revealed cigarette paper scarring over the extensor aspects of both the knee [Figure - 1] and elbow joints. The skin was soft and hyperextensible, particularly over the elbow joints [Figure - 2]. The interphalangeal joints were hypermobile [Figure - 3]. In addition, the younger brother had a high arched palate and the elder brother had kyphoscoliosis [Figure - 4] along with bilateral soft, small-sized testes with decreased testicular sensation. He also had pseudotumor formation around the elbow joints. There was no evidence of purpura, ecchymosis, cyanosis, jaundice, digital clubbing or lymphadenopathy in both the brothers.

The fundus, routine blood tests, urine, coagulogram, blood urea, sugar and serum electrolytes were normal in both the brothers. X-ray skull, barium meal and enema did not show any abnormality in Case 1.

Echocardiography of the elder brother did not reveal any abnormality. Left ventricular ejection fraction was 62 percent and there were no regional wall motion abnormality. All the valves were normal and pliable.

Testicular FNAC revealed decreased spermatogenesis, increased hyalinization and maturation arrest. Hormonal assay revealed serum cortisol at 8 am 12 ug/dl, testosterone 3.2 ng/ml, FSH 26 uI V/ml, LH 18 u IV/ml and serum prolactin 18 ng/ml. Skin biopsy taken from the atrophic skin lesion over the elbow revealed normal epidermis and scanty, whorled, disorderly dermal collagen. Special staining revealed relatively increased and irregularly oriented elastic fibers.

  Discussion Top

A few cases of Ehlers-Danlos syndrome were reported earlier in the Indian literature.[3],[4]

In one case report, Singh et al[5] reported this syndrome in four generations. This genetic disorder has variable prognosis varying from mild to lethal. Its exact etiology is still unknown. Deficiency of some enzymes has been detected in certain types. Several congenital defects like flat feet, myopia, lop ears, prognathism may be associated with this condition.[6] Abnormal bleeding tendency and mitral valve prolapse have also been reported.

The treatment is mainly preventive with avoidance of trauma to prevent cosmetic disfigurement. Vit C has been tried in certain types with some benefit. Plastic surgery can offer some help for the cosmetic improvement. The purpose of reporting these two cases is to create awareness about this condition so that it can be diagnosed early and parents can be counseled at the earliest. Although association of kyphoscoliosis has been reported earlier[7],[8] hyper-gonadotrophic hypogonadism along with testicular failure has not been mentioned, though here, it could be coincidental.

  References Top

1.Burton JL, Lovell CR. Disorders of connective tissue In: Text book of Dermatology, Champion RH, Burton JL, Ebling FJG editors, 6th Ed. Oxford, London: Blackwell Science; 1998. p. 2003-71.  Back to cited text no. 1      
2.Bernett J, Paul H. Congenital diseases (Genodermatoses). In: Lever's Histopathology, David E, Rosalie E, Christine J. Bernett J, editors, 8th Ed. Philadelphia: Lippincott Raven; 1997. p. 117-50.  Back to cited text no. 2      
3.Basak P, Kanwar AJ, Kaur S, Nanda A. Ehlers- Danlos syndrome. Ind J Dermatol Venereol Leprol 1989;55:324-6.  Back to cited text no. 3      
4.Singh SD, Munjal M, Mansharmani RK. Ehlers-Danlos syndrome. Brief review with a case report. Ind J Paediatrics 1964;31:1-2.  Back to cited text no. 4      
5.Singh HB, Saxena HC, Kochar DK, Purohit VP, Singh K, Gupta GK. Ehlers-Danlos syndrome in four generations. Ind J Dermatol Venereol Leprol 1983;49:45-67.  Back to cited text no. 5      
6.Andrew HL, Odom RB, James WD. Abnormalities of dermal connective tissues. In: Andrews Diseases of the Skin 8th Ed. Philadelphia: WB Saunders and Co.; 1990. p. 585-98.  Back to cited text no. 6      
7.Al- Hussain H, Zeisberger SM, Huber PR, Giunta C, Steinmann B. Brittle Cornea syndrome and its delineation from kyphoscoliotic type of Ehlers-Danlos syndrome (EDS VI): Report on 23 patients and review of the literature. Am J Med Genet 2004;124:28-34.  Back to cited text no. 7      
8.Eyre D, Shao P, Weis MA, Steinmann B. The Kyphoscoliotic type of Ehlers-Danlos syndrome (type VI): Differential effect of the hydroxylation of lysine on collagens I and II revealed by analysis of cross linked telopeptides from urine. Mol Genet Metab 2002;76:211-6.  Back to cited text no. 8  [PUBMED]  [FULLTEXT]  


  [Figure - 1], [Figure - 2], [Figure - 3], [Figure - 4]


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