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Related Concept Videos

Imprinting01:22

Imprinting

Behavioral imprinting is observed in some newborn animals and occurs when they develop strong and specific attachments to another animal (usually a parent) following brief, early-life exposures. Offspring imprint onto parents within a brief period after birth or hatching; this time window is called the critical period. Once imprinting occurs, the bond established between the parents and their offspring is usually long-lasting.
Autism Spectrum Disorder01:19

Autism Spectrum Disorder

Autism spectrum disorder (ASD) is a neurodevelopmental condition marked by persistent deficits in social communication and interaction alongside restrictive and repetitive behaviors or interests. ASD is sometimes accompanied by intellectual impairment.
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Atypical gorlin's syndrome.

D Yesudian1, S G Krishnan, M Jayaraman

  • 1Department of Dermatology, Madras Medical College and Goverenment General Hospital, Madras, India, .

Indian Journal of Dermatology, Venereology and Leprology
|October 19, 2010
PubMed
Summary
This summary is machine-generated.

This case study highlights an atypical presentation of Gorlin

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Area of Science:

  • Dermatology
  • Oncology
  • Genetics

Background:

  • Gorlin's syndrome, also known as nevoid basal cell carcinoma syndrome, is a rare genetic disorder.
  • It is characterized by multiple basal cell carcinomas, odontogenic keratocysts, and skeletal abnormalities.
  • Early diagnosis and management are crucial for improving patient outcomes.

Purpose of the Study:

  • To report a rare case of Gorlin's syndrome with an atypical clinical presentation.
  • To emphasize the importance of considering Gorlin's syndrome in patients with unusual skin lesions and a history of keratocysts.
  • To discuss the diagnostic challenges and management strategies for atypical Gorlin's syndrome.

Main Methods:

  • Clinical examination of skin lesions on the face, palms, and soles.
  • Biopsy of skin lesions to confirm basal cell epitheliomas.
  • Review of patient history, including a previous keratocyst removal.
  • Diagnostic confirmation of Gorlin's syndrome based on clinical and pathological findings.

Main Results:

  • A 21-year-old woman presented with facial nodules and palmar/plantar pits.
  • Biopsies confirmed basal cell epitheliomas.
  • The patient had a history of a mandibular keratocyst.
  • The diagnosis of Gorlin's syndrome was made, noted as atypical due to fewer basal cell epitheliomas, a single odontogenic cyst, and absence of other common features.

Conclusions:

  • Gorlin's syndrome can present with atypical features, including a low number of basal cell epitheliomas and odontogenic cysts.
  • This case underscores the need for a comprehensive evaluation in patients with suspected genetic syndromes.
  • Awareness of atypical presentations is essential for accurate diagnosis and timely intervention in Gorlin's syndrome.