Results 151 to 160 of about 1,226,922 (193)
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The Orthopedic Characterization of Goltz Syndrome
American Journal of Medical Genetics, Part C: Seminars in Medical Genetics, 2016Focal dermal hypoplasia (FDH), also known as Goltz syndrome, is a rare condition in which congenital anomalies result in a multitude of defects that affect many systems of the body. These defects can involve the eyes, skin, teeth, and cardiovascular, skeletal, and gastrointestinal systems.
Amanda Smith
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2011
Abstract This chapter provides pictures and clinical details of GOLTZ ...
Charles E. Schwartz +2 more
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Abstract This chapter provides pictures and clinical details of GOLTZ ...
Charles E. Schwartz +2 more
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Journal of Datta Meghe Institute of Medical Sciences University, 2022
Gorlin-Goltz syndrome (GGS) is a rare autosomal dominant condition. Diverse incidence rates of this syndrome have been reported all over the world. It is estimated to occur 1 in 50,000–150,000. GGS is of particular interest to dental surgeons and maxillofacial radiologists because of their association with odontogenic keratocysts (OKC).
Pragati Anupkumar Bhargava +2 more
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Gorlin-Goltz syndrome (GGS) is a rare autosomal dominant condition. Diverse incidence rates of this syndrome have been reported all over the world. It is estimated to occur 1 in 50,000–150,000. GGS is of particular interest to dental surgeons and maxillofacial radiologists because of their association with odontogenic keratocysts (OKC).
Pragati Anupkumar Bhargava +2 more
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Archives of Pediatrics & Adolescent Medicine, 1972
To the Editor .—Several years ago I reported a syndrome 1 which was clearly unusual. To my surprise, pursuit of a diagnosis has led me on an educational journey of syndromes and finally to a definite diagnosis with an improved prognosis for my patient. Essentially, this is a 19-year-old Chinese-American boy who, throughout his life, has had congenital
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To the Editor .—Several years ago I reported a syndrome 1 which was clearly unusual. To my surprise, pursuit of a diagnosis has led me on an educational journey of syndromes and finally to a definite diagnosis with an improved prognosis for my patient. Essentially, this is a 19-year-old Chinese-American boy who, throughout his life, has had congenital
openaire +2 more sources
Examine Your Orofacial Cleft Patients for Gorlin-Goltz Syndrome
Cleft Palate-Craniofacial Journal, 1997 The Gorlin-Goltz syndrome is characterized by four primary symptoms: multiple nevoid basal cell epitheliomas that usually undergo malignant transformation; jaw keratocysts that show constant growth; skeletal anomalies; and intracranial calcifications.
Thomas Kreusch, J Thomas Lambrecht
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Dermoscopy in Gorlin-Goltz Syndrome
Dermatologic Surgery, 2006Gorlin-Goltz syndrome (GGS) is an autosomal dominant disorder mainly characterized by the presence of multiple basal cell carcinomas (BCC), odontogenic keratocysts of the jaw, and volar pits. This syndrome is associated with a wide spectrum of developmental anomalies and neoplasms.To describe dermoscopic characteristics of cutaneous GGS lesions ...
I, Kolm, S, Puig, P, Iranzo, J, Malvehy
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Minerva stomatologica, 2001
The Nevoid Basal Cell Carcinoma Syndrome (NBCCS) or Gorlin-Goltz syndrome, principally characterized by basal cell carcinomas, multiple jaw cysts and skeletal anomalies, is an interesting pathology for the dentist who is often the first clinician involved in the diagnosis of this syndrome.
VESCOVI, Paolo +4 more
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The Nevoid Basal Cell Carcinoma Syndrome (NBCCS) or Gorlin-Goltz syndrome, principally characterized by basal cell carcinomas, multiple jaw cysts and skeletal anomalies, is an interesting pathology for the dentist who is often the first clinician involved in the diagnosis of this syndrome.
VESCOVI, Paolo +4 more
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Acta dermatovenerologica Alpina, Pannonica, et Adriatica, 2007
Gorlin-Goltz syndrome, also known as basal cell nevus syndrome, is an uncommon, autosomal dominant inherited disorder, which is characterized by numerous basal cell carcinomas, maxillary keratocysts, and musculoskeletal malformations. Occasionally, it is associated with aggressive basal cell carcinomas and internal malignancies.
Binić, Ivana +4 more
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Gorlin-Goltz syndrome, also known as basal cell nevus syndrome, is an uncommon, autosomal dominant inherited disorder, which is characterized by numerous basal cell carcinomas, maxillary keratocysts, and musculoskeletal malformations. Occasionally, it is associated with aggressive basal cell carcinomas and internal malignancies.
Binić, Ivana +4 more
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Manifestations of Gorlin-Goltz syndrome.
Danish medical journal, 2014Gorlin-Goltz syndrome is an uncommon hereditary condition caused by mutations in the PTCH1 gene causing a wide range of developmental abnormalities. Multiple basal cell carcinomas, palmoplantar pits and jaw cysts are cardinal features. Many clinicians are unfamiliar with the different manifestations and the fact that patients are especially sensitive ...
Larsen, Anne Kristine +3 more
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2023
Clinical History: A 19-year male patient suffered from road traffic accident and experienced severe pain in the neck. GCS of the patient at presentation was 13/15.
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Clinical History: A 19-year male patient suffered from road traffic accident and experienced severe pain in the neck. GCS of the patient at presentation was 13/15.
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