A Child with Hallermann-Streiff Syndrome; as an Infrequent Cause of Hypotrichosis and Cataract
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Abstract
In present case report, four-months-old boy who referred to our pediatric endocrinology outpatient clinic from department of ophthalmology due to evaluation of endocrine and metabolic disorders for cataract was discussed. The characterized features of patient were hypotrichosis, microphthalmia, nystagmus, strabismus, congenital cataract, beaked nose, micrognathia,
scaphocephaly, frontal and parietal bossing. The case has typical dysmorphic physical examination findings that appropriate diagnostic features to rare Hallermann-Streiff syndrome.
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Hallermannn W. Vogelgesicht und cataracta congenita. Klin. Monatsbl. Augenheilkd. 1948; 113: 315-318.
Streiff EB. Dysmorphie mandibulo-faciale (tete d'oiseau) Alterations oculaires website. Ophthalmologica 1950; 120: 79-83.
François J, Victoria-Troncoso V. François' dyscephalic syndrome and skin manifestations. Ophthalmologica 1981; 183: 63-67.
Steele RW, Bass JW. Hallermann-Streiff syndrome. Clinical and prognostic considerations. Am J Dis Child 1970; 120: 462-465.
Warburg, M. Personal Communication. Copenhagen, Denmark 1971
Grattan CE, Liddle BJ, Willshaw HE. Atrophic alopecia in the Hallermann-Strieff syndrome. Clin Exp Dermatol 1989; 14: 250-252.
Cohen MM Jr. Hallermann-Streiff syndrome: a review. Am J Med Genet 1991; 41: 488-499.
Robinow M. Respiratory obstruction and cor pulmonale in the Hallermann-Streiff syndrome. Am J Med Genet 1991; 41: 515-516.
Hou JW. Hallermann-Streiff syndrome associated with small cerebellum, endocrinopathy and increased chromosomal breakage. Acta Paediatr 2003; 92: 869-871.
Neki AS. Hallermann-Streiff syndrome. Indian J Ophthalmol 1993; 41: 83-84.