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A Child with Hallermann-Streiff Syndrome; as an Infrequent Cause of Hypotrichosis and Cataract

Yıl 2016, Cilt: 3 Sayı: 4, 206 - 8, 15.04.2016

Sultan Kaba , Murat Dogan Nesrin Ceylan , Keziban Bulan Nihat Demir , Sekibe Dogan Selami Kocaman

Öz

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.

Anahtar Kelimeler

Hallermann Streiff Syndrome; congenital cataract; microphthalmia; hypotrichosis

Kaynakça

  • Hallermannn W. Vogelgesicht und cataractacongenita. Klin Monatsbl Augenheilkd. 1948;113:315-318.
  • Streiff EB. Mandibulofacial dysmorphia with ocular abnormalitie. 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 corpulmonale 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.

Medical Science and Discovery

Yıl 2016, Cilt: 3 Sayı: 4, 206 - 8, 15.04.2016

Sultan Kaba , Murat Dogan Nesrin Ceylan , Keziban Bulan Nihat Demir , Sekibe Dogan Selami Kocaman

Öz

Kaynakça

  • Hallermannn W. Vogelgesicht und cataractacongenita. Klin Monatsbl Augenheilkd. 1948;113:315-318.
  • Streiff EB. Mandibulofacial dysmorphia with ocular abnormalitie. 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 corpulmonale 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.
Toplam 10 adet kaynakça vardır.

Ayrıntılar

Birincil Dil İngilizce
Bölüm Vaka Sunumu
Yazarlar

Sultan Kaba

Murat Dogan Bu kişi benim

Nesrin Ceylan

Keziban Bulan Bu kişi benim

Nihat Demir

Sekibe Dogan Bu kişi benim

Selami Kocaman Bu kişi benim

Yayımlanma Tarihi 15 Nisan 2016
Yayımlandığı Sayı Yıl 2016 Cilt: 3 Sayı: 4

Kaynak Göster

APA Kaba, S., Dogan, M., Ceylan, N., Bulan, K., vd. (2016). A Child with Hallermann-Streiff Syndrome; as an Infrequent Cause of Hypotrichosis and Cataract. Medical Science and Discovery, 3(4), 206-8. https://doi.org/10.17546/msd.98327
AMA Kaba S, Dogan M, Ceylan N, Bulan K, Demir N, Dogan S, Kocaman S. A Child with Hallermann-Streiff Syndrome; as an Infrequent Cause of Hypotrichosis and Cataract. Med Sci Discov. Nisan 2016;3(4):206-8. doi:10.17546/msd.98327
Chicago Kaba, Sultan, Murat Dogan, Nesrin Ceylan, Keziban Bulan, Nihat Demir, Sekibe Dogan, ve Selami Kocaman. “A Child With Hallermann-Streiff Syndrome; As an Infrequent Cause of Hypotrichosis and Cataract”. Medical Science and Discovery 3, sy. 4 (Nisan 2016): 206-8. https://doi.org/10.17546/msd.98327.
EndNote Kaba S, Dogan M, Ceylan N, Bulan K, Demir N, Dogan S, Kocaman S (01 Nisan 2016) A Child with Hallermann-Streiff Syndrome; as an Infrequent Cause of Hypotrichosis and Cataract. Medical Science and Discovery 3 4 206–8.
IEEE S. Kaba, M. Dogan, N. Ceylan, K. Bulan, N. Demir, S. Dogan, ve S. Kocaman, “A Child with Hallermann-Streiff Syndrome; as an Infrequent Cause of Hypotrichosis and Cataract”, Med Sci Discov, c. 3, sy. 4, ss. 206–8, 2016, doi: 10.17546/msd.98327.
ISNAD Kaba, Sultan vd. “A Child With Hallermann-Streiff Syndrome; As an Infrequent Cause of Hypotrichosis and Cataract”. Medical Science and Discovery 3/4 (Nisan 2016), 206-8. https://doi.org/10.17546/msd.98327.
JAMA Kaba S, Dogan M, Ceylan N, Bulan K, Demir N, Dogan S, Kocaman S. A Child with Hallermann-Streiff Syndrome; as an Infrequent Cause of Hypotrichosis and Cataract. Med Sci Discov. 2016;3:206–8.
MLA Kaba, Sultan vd. “A Child With Hallermann-Streiff Syndrome; As an Infrequent Cause of Hypotrichosis and Cataract”. Medical Science and Discovery, c. 3, sy. 4, 2016, ss. 206-8, doi:10.17546/msd.98327.
Vancouver Kaba S, Dogan M, Ceylan N, Bulan K, Demir N, Dogan S, Kocaman S. A Child with Hallermann-Streiff Syndrome; as an Infrequent Cause of Hypotrichosis and Cataract. Med Sci Discov. 2016;3(4):206-8.
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