Results 21 to 30 of about 1,226,922 (193)
A family presenting Goltz syndrome (focal dermal hypoplasia) in three generations
The Turkish Journal of Pediatrics, 1998 In this report we present three affected females of the same family in three generations. The cases have features of focal dermal hypoplasia (Goltz syndrome).
M Seven +5 more
doaj +4 more sources
Indian Journal of Paediatric Dermatology, 2016 Goltz syndrome, also known as focal dermal hypoplasia, is a rare genodermatosis. It is an X-linked dominant disorder characterized by mesoectodermal dysplasia present with cutaneous, ocular, dental, and skeletal defects.
Bharati Sahu +3 more
doaj +2 more sources
A case report of focal dermal hypoplasia-Goltz syndrome
Indian Dermatology Online Journal, 2013 Goltz syndrome is a rare multisystem disorder with cutaneous, ocular, dental and skeletal abnormalities. Other mesoectodermal abnormalities are also present. Its hallmark is thinning of the dermis resulting subcutaneous fat herniation.
Sheela Bharani, Sejal Thakkar
doaj +2 more sources
Gorlin Goltz syndrome: A clinicopathological case report
Journal of Indian Academy of Oral Medicine and Radiology, 2014 The Gorlin-Goltz syndrome is an infrequent multisystemic disease, which is inherited in an autosomal dominant manner. This shows a high level of penetrance and variable expressiveness, characterized by multiple basal cell nevi or carcinomas, odontogenic ...
Shobha C Bijjaragi +3 more
doaj +2 more sources
Klinicka Onkologie, 2019 Gorlin-Goltz syndrome is an autosomal dominant inherited disorder characterized by a predisposition to various cancers. Clinicopathological findings of syndrome are very diverse and many symptoms begin to manifest in a certain period of life.The authors describe a case report of a man who, at the age of 34 years, presented to a dermatologist with ...
V, Bartoš +3 more
openaire +2 more sources
Gorlin Goltz syndrome: a rare case report [PDF]
, 2020 Gorlin-Goltz syndrome is uncommon multisystemic disease with an autosomal dominant trait, with complete penetrance and variable expressivity, though sporadic cases have been described.
Gandhi, Mily S. +3 more
core +1 more source
Focal Dermal Hypoplasia: Case Series
Indian Journal of Dermatology, 2023 Background: Focal dermal hypoplasia (Goltz syndrome) is a genetic multisystem disorder characterized primarily by involvement of the skin associated to face, skeletal, and eyes anomalies.
Maria Mansouri +4 more
doaj +1 more source
Türk Pediatri Arşivi, 2017 Gorlin-Goltz syndrome is a rare multisystemic disease inherited in an autosomal dominant pattern. It is characterized by numerous basal cell carcinoma of the skin, jaw cysts, and skeletal anomalies such as frontal bossing, vertebral anomalies, palmoplantar pits, and falx cerebri calcification.
Betül, Şereflican +5 more
openaire +2 more sources
Unilateral Tonsillar Hypertrophy in a 4-Year-Old Girl with Focal Dermal Hypoplasia (Goltz Syndrome)
Philippine Journal of Otolaryngology Head and Neck Surgery, 2018 Objective: To report a case of unilateral tonsillar hypertrophy resulting in severe Obstructive Sleep Apnea in a 4-year-old girl with focal dermal hypoplasia (FDH, Goltz or Goltz-Gorlin) Syndrome. Methods: Design: Case Report Setting:
John Emmanuel L. Ong +2 more
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Oral and Maxillofacial Surgery Cases, 2022 Objective: This case series reports the clinical presentation and management of multiple odontogenic keratocysts (OKCs) in patients with Gorlin Goltz syndrome and in non-syndromic patients.
Omer Sefvan Janjua +4 more
doaj +1 more source