Smith-Lemli-Opitz Syndrome (SLOS): Case Report and Symptomatic Treatment

Taner ÖZTÜRK; Nisa GÜL AMUK

doi:https://doi.org/10.7126/cumudj.492306

Makale detayları

Smith-Lemli-Opitz Syndrome (SLOS): Case Report and Symptomatic Treatment

Yazarlar:

Taner ÖZTÜRK | Nisa GÜL AMUK

Ana Başlıklar:

Sağlık teşvikleri

Dergi:

Cumhuriyet Dental Journal 2019 Vol.22 Issue 2, pp.245-250

Belge Tipi:

Makale

Yayın Tarihi:

5/2019

Belge Dili:

İngilizce

Document ID (Org No.):

2000734601

DOI:

https://doi.org/10.7126/cumudj.492306

Özet:

 


Smith-Lemli-Opitz syndrome is a rare syndrome with multiple congenital anomalies after birth and characteristic with mental retardation. Hereditary cholesterol diseases are an autosomal recessive form of metabolic disturbances. There are two types: Type I with mild clinical signs (classical form) and Type II with severe clinical signs. The Type I form with a higher chance of survival is more common. There are typical craniofacial findings such as microcephaly, low-set ears, micrognathia, flattened nasal root and bitemporal narrowing. Cleft palate and/or deep palate, enlarged alveolar bones, small-sized tongue and swallowing strength are noticeable mouth-related findings. Patients recover at a certain rate with early medical treatment. Early dental treatments are based on eliminating symptomatic problems. A 3-week-old male patient presented with a deep palate, swallowing difficulty, a problem of nourishment, and SLOS Type I was presented.


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Makale detayları

Smith-Lemli-Opitz Syndrome (SLOS): Case Report and Symptomatic Treatment

Yazarlar: Taner ÖZTÜRK | Nisa GÜL AMUK

Ana Başlıklar: Sağlık teşvikleri

Dergi: Cumhuriyet Dental Journal 2019 Vol.22 Issue 2, pp.245-250

Belge Tipi: Makale

Yayın Tarihi: 5/2019

Belge Dili: İngilizce

Document ID (Org No.): 2000734601

DOI: https://doi.org/10.7126/cumudj.492306

Sayı

Yazarlar:

Taner ÖZTÜRK | Nisa GÜL AMUK

Ana Başlıklar:

Sağlık teşvikleri

Dergi:

Cumhuriyet Dental Journal 2019 Vol.22 Issue 2, pp.245-250

Belge Tipi:

Makale

Yayın Tarihi:

5/2019

Belge Dili:

İngilizce

Document ID (Org No.):

2000734601

DOI:

https://doi.org/10.7126/cumudj.492306