Haber syndrome - Wikipedia
Haber syndrome is a cutaneous disorder of hyperpigmentation characterized by reticulated pigmentation of the person's skin. [1] A rare genodermatosis, [2] its key features include "rosacea-like facial eruption[,] reticulated hyperpigmentation of major flexures, comedones on the back and neck, and pitted facial scars." [1]
Haber's syndrome - PubMed
Haber's syndrome is a rare genodermatosis characterised by an early onset rosacea-like eruption associated with multiple truncal keratotic lesions. The present study reports the clinical presentation, histology and response to therapy of two cases of Haber's syndrome.
Haber Syndrome - SpringerLink
Haber syndrome is a rare genodermatosis characterized by a familial occurrence, a rosacea-like eruption of the face, multiple truncal keratotic lesions, and small pitted scars of the face. The rosacea-like dermatosis has the clinical features of an erythematous...
Haber Syndrome（哈伯综合征、表皮内上皮瘤酒渣鼻样疹） - 皮 …
哈伯综合征（Haber Syndrome）又称表皮内上皮瘤-酒渣鼻样疹（intraepidermal epithelioma-rosacea like eruption）、家族性酒渣鼻样疹伴表皮内上皮瘤（familial rosacea-like eruption with intraepithelial epithelioma）。为常染色体显性遗传。 临床症状. 两耳均可受累，儿童时期发病。
Dowling-Degos disease pathology - DermNet
Haber syndrome — shared histological features with Dowling-Degos disease; however, the clinical presentation is distinct with facial rosacea-like lesions, pitted scars and seborrhoeic keratosis-like lesions in the trunk and flexures. Haber syndrome is not associated with keratin 5 mutations. Dermatology (Third edition, 2012).
Haber syndrome (Concept Id: C0263450) - National Center for ...
Heterozygous variants in MYH10 associated with neurodevelopmental disorders and congenital anomalies with evidence for primary cilia-dependent defects in Hedgehog signaling.
Haber’s syndrome may be a clinical entity different from …
2009年1月1日 · S ir, Haber’s syndrome (HS) is a rare genodermatosis that was first described by Sanderson and Wilson. 1 The disease is thought to be autosomal dominant and only 14 cases from seven families have been described. Clinically, HS is associated with a rosacea‐like eruption of the face that begins in childhood, and profuse keratotic lesions ...
Haber syndrome, Dowling-Degos disease, and Kitamura disease (reticulate acropig mentation) form a spectrum of autosomal dominant genodermatoses characterized by varying expressions of reticulate pig mentation, follicular plugging, and scar ring. Haber syndrome may be interpreted as a combination of Dowling-Degos disease
Haber syndrome - VisualDx
2023年8月26日 · Haber syndrome is an extremely rarely reported, autosomal-dominant genodermatosis characterized by an early-onset, persistent, photosensitive, rosacea -like facial eruption and multiple dark brown, seborrheic keratosis -like papules affecting the flexures and intertriginous areas, and the trunk more diffusely in more severe cases.
Haber's Syndrome: A Case Report - PubMed
2023年2月13日 · Haber's syndrome is an autosomal dominant, rare genodermatosis characterized by photosensitive, persistent facial erythema associated with reticulated hyperpigmentation. We present a case of an eight-year-old healthy Saudi girl who presented with facial erythema and generalized reticulated hyperpigm …