Results 121 to 130 of about 7,109,345 (167)
Successful Treatment of Acrodermatitis Continua of Hallopeau With Tildrakizumab: A Case Report
SAGE Open Medical Case Reports, 2023 Acrodermatitis continua of Hallopeau is a rare, localized variant of pustular psoriasis commonly associated with join disease and severe quality of life impairment.
Alex Nguyen +2 more
exaly +2 more sources
Acrodermatitis Continua of Hallopeau Successfully Treated With Adalimumab: A Case Report
SAGE Open Medical Case Reports, 2019 Acrodermatitis continua of Hallopeau is a chronic, inflammatory, and relapsing condition that presents as pustules of the fingers and toes, often with nail involvement.
Melinda Gooderham, Ashley O'Toole
exaly +2 more sources
Dermatologic Therapy, 2019 Acrodermatitis continua of Hallopeau (ACH) is a rare pustular psoriasis variant refractory to many conventional treatments. We report the successful treatment with secukinumab of a patient with a long history of ACH with marked onychodystrophy with frank
Luca Bianchi +2 more
exaly +2 more sources
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International Journal of Dermatology, 1984
ABSTRACT: Two cases of pemphigus vegetans are presented, one of the Neumann type and one of the Hallopeau type. The differences between the two subsets are clinical presentation and course. Patients with the Hallopeau type often have a relatively benign disease, require lower doses of systemic corticosteroids, and usually have a prolonged remission ...
A R, Ahmed, D A, Blose
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ABSTRACT: Two cases of pemphigus vegetans are presented, one of the Neumann type and one of the Hallopeau type. The differences between the two subsets are clinical presentation and course. Patients with the Hallopeau type often have a relatively benign disease, require lower doses of systemic corticosteroids, and usually have a prolonged remission ...
A R, Ahmed, D A, Blose
openaire +2 more sources
Obstetrics & Gynecology, 1997
Epidermolysis bullosa dystrophica of the mutilating Hallopeau-Siemens type is a rare inherited skin disease. Those afflicted have blisters and pronounced scarring of skin and mucous membranes after minor trauma. Pregnancies are very rare in affected women.A 24-year-old woman, gravida 1, with a severe form of the Hallopeau-Siemens type was monitored ...
U, Büscher +3 more
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Epidermolysis bullosa dystrophica of the mutilating Hallopeau-Siemens type is a rare inherited skin disease. Those afflicted have blisters and pronounced scarring of skin and mucous membranes after minor trauma. Pregnancies are very rare in affected women.A 24-year-old woman, gravida 1, with a severe form of the Hallopeau-Siemens type was monitored ...
U, Büscher +3 more
openaire +3 more sources
Acrodermatitis Continua of Hallopeau: Clinical Perspectives [PDF]
Psoriasis: Targets and Therapy, 2019 Acrodermatitis continua of Hallopeau (ACH) is a rare, sterile pustular eruption of one or more digits. The condition presents with tender pustules and underlying erythema on the tip of a digit, more frequently arising on a finger than a toe.
Quinn Thibodeaux +2 more
exaly +2 more sources
British Journal of Dermatology, 1993
The serum of a 34-year-old woman with the Hallopeau type of pemphigus vegetans (PVg) contained antibodies against a 130-kDa polypeptide in human epidermal lysates, as revealed by Western blot analysis. The serum strongly fixed complement in vitro, and the PVg lesional skin contained a predominance of complement-fixing IgG2 and IgG4.
H, Hashizume, K, Iwatsuki, M, Takigawa
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The serum of a 34-year-old woman with the Hallopeau type of pemphigus vegetans (PVg) contained antibodies against a 130-kDa polypeptide in human epidermal lysates, as revealed by Western blot analysis. The serum strongly fixed complement in vitro, and the PVg lesional skin contained a predominance of complement-fixing IgG2 and IgG4.
H, Hashizume, K, Iwatsuki, M, Takigawa
openaire +2 more sources
Ocular lesions in generalized hallopeau-siemens type of recessive dystrophic epidermolysis bullosa
Annals of Ophthalmology, 2001An infant was given a diagnosis of the Hallopeau-Siemens type recessive dystrophic epidermolysis bullosa shortly after birth, based on clinical, hereditary, and ultrastructural findings. At age 10 years, the boy complained of mild ocular pain. On examination, corneal opacities; erosion and blister in an eyelid; symblepharon; and occlusion of both upper
Yoriko Hayasaka +4 more
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Nature Genetics, 1993
The Hallopeau-Siemens type of recessive dystrophic epidermolysis bullosa (HS-RDEB) is a life-threatening autosomal disease characterized by loss of dermal-epidermal adherence with abnormal anchoring fibrils (AF). We recently linked HS-RDEB to the type VII collagen gene (COL7A1) which encodes the major component of AF.
Latifa Hilal +10 more
openaire +4 more sources
The Hallopeau-Siemens type of recessive dystrophic epidermolysis bullosa (HS-RDEB) is a life-threatening autosomal disease characterized by loss of dermal-epidermal adherence with abnormal anchoring fibrils (AF). We recently linked HS-RDEB to the type VII collagen gene (COL7A1) which encodes the major component of AF.
Latifa Hilal +10 more
openaire +4 more sources
[Pemphigus vegetans, a clinical type of chronic pustular dermatitis of Hallopeau].
Annales de dermatologie et de venereologie, 1983A 49-year old woman had an eruption resembling 'dermatite pustuleuse chronique en foyers a progression excentrique' as initially described by Hallopeau. Numberous vegetating lesions occurred over the genitocrural, pubic, umbilical and submammary regions. The finger-nails showed onycholysis and sterile pustules.
D, Leroy +4 more
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