A case of acrogeria-a rare premature ageing syndrome

Tahir Shehzad, Naveed Illahi

Abstract


A case of acrogeria of a 9-month-old boy is reported here who presented with dry, scaly skin, birdlike facies, prominent frontal tuberosities, recessed chin, dry, thin skin with generalized subcutaneous fat loss, prominent veins, prominent eyes, thin and brittle nails, poorly developed musculature and hair loss at the back of scalp.


Keywords


Premature ageing syndromes, progeria, acrogeria, pangeria

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References


Beauregard S. Gilchrist BA. Syndrome of premature ageing. Dermatol Clin 1987; 5: 109-21.

Martin GM, Oshima J. Lessons from human progeroid syndrome. Nature 2000; 408: 263-6.

Badame AJ. Progeria. Arch Dermatol 1989; 125: 540-4.

Martin GM. Syndromes of accelerated ageing. NCI Monogr 1982; 60: 241-7.

Gottron H. Familiare Akrogeria. Arch Dermatol 1941; 181: 571- 83.

De Groot WP, Tafelkruyer J, Woerdeman MJ. Familial acrogeria. Br J Dermatol 1980; 103: 213-23.

Jansen T, De Paepe, Luytinck N, Plewig G. COL3A1 mutations leading to acrogeria. Br J Dermatol 2000; 142: 178-9.

Goldstein S. Studies on age-related diseases in cultured fibroblasts. J Invest Dermatol 1979; 73: 19-23.


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