Abstract
A 3-d-old female baby presented with bilateral congenital absence of breast tissue, areolae and nipples. No other anomalies were noted. There was also a history of absence of nipples, areolae and breast tissue in the mother and two other family members of maternal side. Investigations done during the hospital stay including ultrasound of the chest wall, abdomen and head were all normal. Congenital isolated bilateral amastia was diagnosed after complete investigations.
References
Bianca S, Licciardello M, Barrano B, Ettore G. Isolated congenital amastia: a subclavian artery supply disruption sequence? Am J Med Genet A. 2010;152A:792–4.
Wylie W. A case of entire absence of both mammae in a female aged 21 years. B Med J. 1885;2:235.
Fraser FC. Dominant inheritance of absent nipples and breasts. In: Novant’Anni Delle Leggi Mendeliane ed. Rome: Istituto Gregorio Mendel (pub.); 1956. pp. 360–2.
Goldenring H, Crelin ES. Mother and daughter with bilateral congenital amastia. Yale J Biol Med. 1961;33:466–7.
Pinheiro M, Freire-Maia N, Chautard-Freiren-Maia EA, et al. AREDYLD: A syndrome combining an acro-renal field defect, ectodermal dysplasia, lipoatrophic diabetes and other manifestations. Am J Med Genet. 1983;16:29–33.
Merlob P. Congenital malformations and development changes of the breast: a neonatological view. J Pediatr Endocrinol Metabol. 2003;16:471–85.
Kowlessar M, Orti E. Complete breast absence in siblings. Am J Dis Child. 1968;115:91–2.
Bouvet JP, Leveque D, Bernetiers F, Gros JJ. Vascular origin of Poland syndrome? A comparative rheographic study of the vascularisation of the arms in eight patients. Eur J Pediatr. 1978;128:17–26.
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Patil, L.G.C., Shivanna, N.H., Benakappa, N. et al. Congenital Amastia. Indian J Pediatr 80, 870–871 (2013). https://doi.org/10.1007/s12098-012-0919-1
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DOI: https://doi.org/10.1007/s12098-012-0919-1