Horner Syndrome With a Positive Harlequin Sign in an Adolescent Male
No abstract available (Source: Journal of Neuro-Ophthalmology)
Source: Journal of Neuro-Ophthalmology - November 26, 2022 Category: Opthalmology Tags: Clinical Correspondence Source Type: research
Hidden Harlequin syndrome in neonatal and pediatric VA-ECMO
(Source: Critical Care)
Source: Critical Care - May 20, 2022 Category: Intensive Care Authors: Yael Levy, Julie Starck, Anne-Lise Mary, Yohan Soreze, Sandrine Jean, Bernard Kreitmann, Pierre-Louis L éger and Jerome Rambaud Tags: Correspondence Source Type: research
Harlequin syndrome: An asymmetric face
AbstractHarlequin syndrome corresponds to unilateral dysfunction of the sympathetic system, characterized by flush and unilateral hyperhidrosis associated with hypo or anhidrosis and paleness of the opposite side. It is, usually, idiopathic. Rarely, it may be associated with compressive organic processes, iatrogenic causes, and general diseases. It is a real therapeutic challenge. (Source: Clinical Case Reports)
Source: Clinical Case Reports - May 12, 2022 Category: General Medicine Authors: Mouna Korbi,
Sirine Boumaiza,
Asma Achour,
Hichem Belhadjali,
Jameleddine Zili Tags: CASE REPORT Source Type: research
SCN10A variants associated with congenital Harlequin Syndrome
Br J Dermatol. 2022 Jan 10. doi: 10.1111/bjd.21011. Online ahead of print.NO ABSTRACTPMID:35007332 | DOI:10.1111/bjd.21011 (Source: The British Journal of Dermatology)
Source: The British Journal of Dermatology - January 10, 2022 Category: Dermatology Authors: Aurelie Halle Alix De Becdelievre Benoit Funalot Christine Labr èze Fanny Morice-Picard Franck Boralevi Source Type: research
SCN10A variants associated with congenital Harlequin Syndrome
Br J Dermatol. 2022 Jan 10. doi: 10.1111/bjd.21011. Online ahead of print.NO ABSTRACTPMID:35007332 | DOI:10.1111/bjd.21011 (Source: The British Journal of Dermatology)
Source: The British Journal of Dermatology - January 10, 2022 Category: Dermatology Authors: Aurelie Halle Alix De Becdelievre Benoit Funalot Christine Labr èze Fanny Morice-Picard Franck Boralevi Source Type: research
SCN10A variants associated with congenital Harlequin Syndrome
Br J Dermatol. 2022 Jan 10. doi: 10.1111/bjd.21011. Online ahead of print.NO ABSTRACTPMID:35007332 | DOI:10.1111/bjd.21011 (Source: The British Journal of Dermatology)
Source: The British Journal of Dermatology - January 10, 2022 Category: Dermatology Authors: Aurelie Halle Alix De Becdelievre Benoit Funalot Christine Labr èze Fanny Morice-Picard Franck Boralevi Source Type: research
Harlequin syndrome after surgery for aortic dissection
(Source: Intensive Care Medicine)
Source: Intensive Care Medicine - November 27, 2021 Category: Intensive Care Source Type: research
Harlequin syndrome, apnea, and acute on chronic hemiparesis: an atypical pediatric case of Chiari I with holocord syringohydromyelia
A four-year-old, right handed, full term female, with mild global developmental delay, presented to the emergency department for evaluation of progressive right hemiparesis. Her development was significant for walking at 18 months and expressive speech delay. At 3.5 years old, she was diagnosed with Harlequin syndrome (Figure 1) after multiple episodes of left hemifacial flushing with physical exertion. Concurrently, she began dragging her right leg, and was diagnosed with hemiplegic cerebral palsy by an outside hospital. (Source: Pediatric Neurology)
Source: Pediatric Neurology - October 25, 2021 Category: Neurology Authors: Stephen Chrzanowski, Alexandra Baker, Leslie Hayes, Hanalise V. Huff, Lauren Fanty, Mark Proctor, Edward Yang, Kelsey Miller, Kiran Maski Tags: Short Communication Source Type: research
Vitamin D Status in Distinct Types of Ichthyosis: Importance of Genetic Type and Severity of Scaling
This study determined serum levels of 25-hydroxyvitamin D3 (25(OH)D3) in 87 patients with ichthyosis; 69 patients were additionally analysed for parathyroid hormone. Vitamin D deficiency was pronounced in keratinopathic ichthyosis (n = 17; median 25(OH)D3: 10.5 ng/ml), harlequin ichthyosis (n = 2;7.0 ng/ml) and rare syndromic subtypes (n = 3; 7.0 ng/ml). Vitamin D levels were reduced in TG1-proficient lamellar ichthyosis (n = 15; 11.9 ng/ml), TG1-deficient lamellar ichthyosis (n = 12; 11.7 ng/ml), congenital ichthyosiform erythroderma (n = 13; 12.4 ng/ml), Netherton syndrome (n = 7; 10.7 ng/ml) and X-linked ichthyosis (n =...
Source: Acta Dermato-Venereologica - August 16, 2021 Category: Dermatology Authors: Mi-Ran Kim Vinzenz Oji Frederic Valentin Heiko Traupe Jerzy-Roch Nofer Ingrid Hausser Hans Christian Hennies Katja Eckl Stefan A Wudy Alberto S ánchez-Guijo Laura Kerschke Judith Fischer Kira S üssmuth Source Type: research
Vitamin D Status in Distinct Types of Ichthyosis: Importance of Genetic Type and Severity of Scaling
This study determined serum levels of 25-hydroxyvitamin D3 (25(OH)D3) in 87 patients with ichthyosis; 69 patients were additionally analysed for parathyroid hormone. Vitamin D deficiency was pronounced in keratinopathic ichthyosis (n = 17; median 25(OH)D3: 10.5 ng/ml), harlequin ichthyosis (n = 2;7.0 ng/ml) and rare syndromic subtypes (n = 3; 7.0 ng/ml). Vitamin D levels were reduced in TG1-proficient lamellar ichthyosis (n = 15; 11.9 ng/ml), TG1-deficient lamellar ichthyosis (n = 12; 11.7 ng/ml), congenital ichthyosiform erythroderma (n = 13; 12.4 ng/ml), Netherton syndrome (n = 7; 10.7 ng/ml) and X-linked ichthyosis (n =...
Source: Acta Derm Venereol A... - August 16, 2021 Category: Dermatology Authors: Mi-Ran Kim Vinzenz Oji Frederic Valentin Heiko Traupe Jerzy-Roch Nofer Ingrid Hausser Hans Christian Hennies Katja Eckl Stefan A Wudy Alberto S ánchez-Guijo Laura Kerschke Judith Fischer Kira S üssmuth Source Type: research
Vitamin D Status in Distinct Types of Ichthyosis: Importance of Genetic Type and Severity of Scaling
This study determined serum levels of 25-hydroxyvitamin D3 (25(OH)D3) in 87 patients with ichthyosis; 69 patients were additionally analysed for parathyroid hormone. Vitamin D deficiency was pronounced in keratinopathic ichthyosis (n = 17; median 25(OH)D3: 10.5 ng/ml), harlequin ichthyosis (n = 2;7.0 ng/ml) and rare syndromic subtypes (n = 3; 7.0 ng/ml). Vitamin D levels were reduced in TG1-proficient lamellar ichthyosis (n = 15; 11.9 ng/ml), TG1-deficient lamellar ichthyosis (n = 12; 11.7 ng/ml), congenital ichthyosiform erythroderma (n = 13; 12.4 ng/ml), Netherton syndrome (n = 7; 10.7 ng/ml) and X-linked ichthyosis (n =...
Source: Acta Dermato-Venereologica - August 16, 2021 Category: Dermatology Authors: Mi-Ran Kim Vinzenz Oji Frederic Valentin Heiko Traupe Jerzy-Roch Nofer Ingrid Hausser Hans Christian Hennies Katja Eckl Stefan A Wudy Alberto S ánchez-Guijo Laura Kerschke Judith Fischer Kira S üssmuth Source Type: research
Vitamin D Status in Distinct Types of Ichthyosis: Importance of Genetic Type and Severity of Scaling
This study determined serum levels of 25-hydroxyvitamin D3 (25(OH)D3) in 87 patients with ichthyosis; 69 patients were additionally analysed for parathyroid hormone. Vitamin D deficiency was pronounced in keratinopathic ichthyosis (n = 17; median 25(OH)D3: 10.5 ng/ml), harlequin ichthyosis (n = 2;7.0 ng/ml) and rare syndromic subtypes (n = 3; 7.0 ng/ml). Vitamin D levels were reduced in TG1-proficient lamellar ichthyosis (n = 15; 11.9 ng/ml), TG1-deficient lamellar ichthyosis (n = 12; 11.7 ng/ml), congenital ichthyosiform erythroderma (n = 13; 12.4 ng/ml), Netherton syndrome (n = 7; 10.7 ng/ml) and X-linked ichthyosis (n =...
Source: Acta Derm Venereol A... - August 16, 2021 Category: Dermatology Authors: Mi-Ran Kim Vinzenz Oji Frederic Valentin Heiko Traupe Jerzy-Roch Nofer Ingrid Hausser Hans Christian Hennies Katja Eckl Stefan A Wudy Alberto S ánchez-Guijo Laura Kerschke Judith Fischer Kira S üssmuth Source Type: research
Vitamin D Status in Distinct Types of Ichthyosis: Importance of Genetic Type and Severity of Scaling
This study determined serum levels of 25-hydroxyvitamin D3 (25(OH)D3) in 87 patients with ichthyosis; 69 patients were additionally analysed for parathyroid hormone. Vitamin D deficiency was pronounced in keratinopathic ichthyosis (n = 17; median 25(OH)D3: 10.5 ng/ml), harlequin ichthyosis (n = 2;7.0 ng/ml) and rare syndromic subtypes (n = 3; 7.0 ng/ml). Vitamin D levels were reduced in TG1-proficient lamellar ichthyosis (n = 15; 11.9 ng/ml), TG1-deficient lamellar ichthyosis (n = 12; 11.7 ng/ml), congenital ichthyosiform erythroderma (n = 13; 12.4 ng/ml), Netherton syndrome (n = 7; 10.7 ng/ml) and X-linked ichthyosis (n =...
Source: Acta Dermato-Venereologica - August 16, 2021 Category: Dermatology Authors: Mi-Ran Kim Vinzenz Oji Frederic Valentin Heiko Traupe Jerzy-Roch Nofer Ingrid Hausser Hans Christian Hennies Katja Eckl Stefan A Wudy Alberto S ánchez-Guijo Laura Kerschke Judith Fischer Kira S üssmuth Source Type: research
Successful treatment of idiopathic Harlequin Syndrome with oxybutynin and propranolol
We present the case of a patient with idiopathic HS successfully treated with oxybutynin and propranolol. In this patient, a marked improvement in both hyperhidrosis and facial erythema was noted with this combined therapy. We consider it of interest to highlight the response of our patient to the treatment employed, which may be advantageous in future cases of this rare disorder.PMID:34314021 | DOI:10.1111/ajd.13665 (Source: The Australasian Journal of Dermatology)
Source: The Australasian Journal of Dermatology - July 27, 2021 Category: Dermatology Authors: Cristina Naharro-Fern ández Adri án de Quintana-Sancho Ana Elizabet L ópez-Sundh Leandra Reguero-Del Cura Marcos A G ónzalez-López Source Type: research
Successful treatment of idiopathic Harlequin Syndrome with oxybutynin and propranolol
We present the case of a patient with idiopathic HS successfully treated with oxybutynin and propranolol. In this patient, a marked improvement in both hyperhidrosis and facial erythema was noted with this combined therapy. We consider it of interest to highlight the response of our patient to the treatment employed, which may be advantageous in future cases of this rare disorder.PMID:34314021 | DOI:10.1111/ajd.13665 (Source: The Australasian Journal of Dermatology)
Source: The Australasian Journal of Dermatology - July 27, 2021 Category: Dermatology Authors: Cristina Naharro-Fern ández Adri án de Quintana-Sancho Ana Elizabet L ópez-Sundh Leandra Reguero-Del Cura Marcos A G ónzalez-López Source Type: research
