Recurrent congenital double upper lip: A case report

Uchikawa, Eri; Yoshizawa, Michiko; Funayama, Akinori; Mikami, Toshihiko; Kobayashi, Tadaharu

doi:10.1016/j.ajoms.2017.11.010

Journal of Oral and Maxillofacial Surgery, Medicine, and Pathol

2018

DOI: 10.1016/j.ajoms.2017.11.010

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Recurrent congenital double upper lip: A case report

Eri Uchikawa

Michiko Yoshizawa

Akinori Funayama

et al.

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2024

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Bilabial double lip with blepharochalasis in Laffer‐Aschers syndrome: Report of a rare association

Ujjya,

Lonyal,

Singh

et al. 2024

Oral Science International

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BackgroundLaffer‐Aschers syndrome (LAS), a rare congenital idiopathic condition, is characterized by double upper lip, recurrent edema of upper eyelids (blepharochalasis), and occasional nontoxic goiter (NTG).Case PresentationTwo rare cases of bilabial double lip involvement in LAS are presented in young males with blepharochalasis, causing aesthetic concerns and requiring surgical correction for rehabilitation. Evaluation for NTG was negative in both cases. A rare association with alopecia areata was also noted in one case, reported only once before.ConclusionThe etiology, clinical features, differential diagnosis, investigations, and management are discussed with review of literature of bilabial double lip in LAS.

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Bilabial double lip with blepharochalasis in Laffer‐Aschers syndrome: Report of a rare association

Ujjya,

Lonyal,

Singh

et al. 2024

Oral Science International

View full text Add to dashboard Cite

show abstract

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Recurrent congenital double upper lip: A case report

Cited by 1 publication

References 12 publications

Bilabial double lip with blepharochalasis in Laffer‐Aschers syndrome: Report of a rare association

Bilabial double lip with blepharochalasis in Laffer‐Aschers syndrome: Report of a rare association

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