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Hypertrichosis

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1. Plexiform Schwannoma with Localized Hypertrichosis (PubMed)

Plexiform Schwannoma with Localized Hypertrichosis 30065605 2018 11 14 1013-9087 30 4 2018 Aug Annals of dermatology Ann Dermatol Plexiform Schwannoma with Localized Hypertrichosis. 508-509 10.5021/ad.2018.30.4.508 Kim Woo-Il WI Department of Dermatology, Pusan National University School of Medicine, Busan, Korea. Department of Dermatology, Pusan National University Yangsan Hospital, Yangsan, Korea. Kim Tae-Wook TW Department of Dermatology, Pusan National University School of Medicine, Busan

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2018 Annals of dermatology

2. Hypertrichosis of the pinnae in a patient using panitumumab. (PubMed)

Hypertrichosis of the pinnae in a patient using panitumumab. 29377278 2018 06 26 1468-3083 32 7 2018 Jul Journal of the European Academy of Dermatology and Venereology : JEADV J Eur Acad Dermatol Venereol Hypertrichosis of the pinnae in a patient using panitumumab. e277-e278 10.1111/jdv.14815 Baykal C C Department of Dermatology and Venereology, Istanbul Medical Faculty, Istanbul University, Istanbul, Turkey. Babuna Kobaner G G Department of Dermatology and Venereology, Istanbul Medical Faculty

2018 Journal of the European Academy of Dermatology and Venereology

3. The First Reported Case of Fibrous Hamartoma of Infancy with Hyperhidrosis and Hypertrichosis in Korea (PubMed)

The First Reported Case of Fibrous Hamartoma of Infancy with Hyperhidrosis and Hypertrichosis in Korea Fibrous hamartoma of infancy (FHI) is a rare entity with a benign nature. The typical clinical features are a single, slowly growing, painless mass on the trunk that appears within the first 2 years of life. We report a 13-month-old boy who presented with a plaque on the lower back since 4 months of age. The plaque had gradually become larger and firm, and hyperhidrosis and hypertrichosis were (...) noticed. No visible connection between the spinal cord and the lesion was found in radiologic studies, indicating a disease other than spinal dysraphism. Histopathological findings showed well-defined fibrous trabeculae, mature adipose tissue, and primitive mesenchymal cells, all consistent with FHI. This is the first case of FHI presenting with hyperhidrosis and hypertrichosis reported in Korea.© 2018 The Korean Academy of Medical Sciences.

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2018 Journal of Korean medical science

4. Novel mutation in ABBC9 gene associated with congenital hypertrichosis and acromegaloid facial features, without cardiac or skeletal anomalies: a new phenotype (PubMed)

Novel mutation in ABBC9 gene associated with congenital hypertrichosis and acromegaloid facial features, without cardiac or skeletal anomalies: a new phenotype Mutations in ABCC9 are associated with Cantú syndrome (CS), a very rare genetic disorder characterized by congenital hypertrichosis, acromegaloid facial appearance (AFA), cardiomegaly, and skeletal anomalies.We report an 8-year-old female patient with congenital generalized hypertrichosis and coarse facial appearance but without (...) cardiovascular or skeletal compromise. Whole exome sequencing revealed a novel de novo heterozygous mutation in ABCC9. In addition, the genotype and phenotype of the patient were compared with those of the patients reported in the literature and with other related conditions that include AFA, hypertrichosis and AFA, and CS.This is the first report of a South-American patient with mutation in ABCC9. We propose that her phenotype is a part of a spectrum of features associated with congenital hypertrichosis

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2018 The application of clinical genetics

5. De Novo Mutations in SLC25A24 Cause a Craniosynostosis Syndrome with Hypertrichosis, Progeroid Appearance, and Mitochondrial Dysfunction. (PubMed)

De Novo Mutations in SLC25A24 Cause a Craniosynostosis Syndrome with Hypertrichosis, Progeroid Appearance, and Mitochondrial Dysfunction. Gorlin-Chaudhry-Moss syndrome (GCMS) is a dysmorphic syndrome characterized by coronal craniosynostosis and severe midface hypoplasia, body and facial hypertrichosis, microphthalmia, short stature, and short distal phalanges. Variable lipoatrophy and cutis laxa are the basis for a progeroid appearance. Using exome and genome sequencing, we identified

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2017 American Journal of Human Genetics

6. Congenital Linear Smooth Muscle Hamartoma with Hypertrichosis: Hair Density on Dermoscopy in Parallel with the Number of Smooth Muscle Bundles (PubMed)

Congenital Linear Smooth Muscle Hamartoma with Hypertrichosis: Hair Density on Dermoscopy in Parallel with the Number of Smooth Muscle Bundles 29386851 2018 11 13 1013-9087 30 1 2018 Feb Annals of dermatology Ann Dermatol Congenital Linear Smooth Muscle Hamartoma with Hypertrichosis: Hair Density on Dermoscopy in Parallel with the Number of Smooth Muscle Bundles. 114-116 10.5021/ad.2018.30.1.114 Son Jin-Hwa JH Department of Dermatology, Pusan National University School of Medicine, Busan, Korea

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2017 Annals of dermatology

7. The HHID syndrome of hypertrichosis, hyperkeratosis, abnormal corpus callosum, intellectual disability, and minor anomalies is caused by mutations in ARID1B (PubMed)

The HHID syndrome of hypertrichosis, hyperkeratosis, abnormal corpus callosum, intellectual disability, and minor anomalies is caused by mutations in ARID1B 28323383 2018 06 21 2018 11 13 1552-4833 173 5 2017 May American journal of medical genetics. Part A Am. J. Med. Genet. A The HHID syndrome of hypertrichosis, hyperkeratosis, abnormal corpus callosum, intellectual disability, and minor anomalies is caused by mutations in ARID1B. 1440-1443 10.1002/ajmg.a.38143 Zweier Markus M Institute (...) genetics Child DNA-Binding Proteins genetics Facies Female Genetic Association Studies Humans Hyperkeratosis, Epidermolytic diagnosis genetics Hypertrichosis diagnosis genetics Intellectual Disability diagnosis genetics Mutation Phenotype Transcription Factors genetics Whole Exome Sequencing Young Adult ARID1B Coffin-Siris syndrome HHID abnormal corpus callosum hyperkeratosis hypertrichosis intellectual disability minor anomalies 2016 12 21 2016 12 22 2017 3 23 6 0 2018 6 22 6 0 2017 3 22 6 0 ppublish

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2017 American journal of medical genetics. Part A

8. Anterior cervical hypertrichosis: a sporadic case (PubMed)

Anterior cervical hypertrichosis: a sporadic case Anterior cervical hypertrichosis is a very rare form of primary localized hypertrichosis. It consists of a tuft of terminal hair on the anterior neck just above the laryngeal prominence. The etiology is still unknown. In this article, we reported a 15-year-old female patient who presented to our clinic with a complaint of hypertrichosis on the anterior aspect of the neck for the last five years. Her past medical history revealed no pathology (...) except for vesicoureteral reflux. On the basis of clinical presentation, our patient was diagnosed with anterior cervical hypertrichosis and she was considered to be a sporadic case due to lack of other similar cases in familial history. To date, 33 patients with anterior cervical hypertrichosis have been reported. Anterior cervical hypertrichosis can be associated with other abnormalities, but it frequently presents as an isolated defect (70%). The association of vesicoureteral reflux and anterior

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2016 Turkish Archives of Pediatrics/Türk Pediatri Arşivi

9. Acquired Localized Hypertrichosis Induced by Rivastigmine (PubMed)

Acquired Localized Hypertrichosis Induced by Rivastigmine Hypertrichosis is the excessive hair growth in any area of the skin surface. Acquired localized hypertrichosis may be secondary to multiple causes and there is a secondary form due to several drugs, which is usually reversible with discontinuation of the causative agent. Rivastigmine is a reversible and competitive inhibitor of acetylcholinesterase and butyrylcholinesterase used for symptomatic treatment of Alzheimer dementia (...) and Parkinson's disease. It has an adequate safety profile and cutaneous side effects are unusual. Irritant contact dermatitis, allergic dermatitis, baboon syndrome, and cutaneous rash due to rivastigmine have been reported. We report on a Caucasian 80-year-old male with personal history of Alzheimer's disease. The patient started therapy with oral rivastigmine one month prior to clinical presentation of localized hypertrichosis on both forearms. Norgalanthamine has been shown to promote hair growth activity

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2016 Case reports in dermatological medicine

10. Hypertrichosis

Hypertrichosis Hypertrichosis Toggle navigation Brain Head & Neck Chest Endocrine Abdomen Musculoskeletal Skin Infectious Disease Hematology & Oncology Cohorts Diagnostics Emergency Findings Procedures Prevention & Management Pharmacy Resuscitation Trauma Emergency Procedures Ultrasound Cardiovascular Emergencies Lung Emergencies Infectious Disease Pediatrics Neurologic Emergencies Skin Exposure Miscellaneous Abuse Cancer Administration 4 Hypertrichosis Hypertrichosis Aka: Hypertrichosis From (...) Related Chapters II. Definition s Non-pigmented fine "peach fuzz" hair covering body Found in children and adults Hypertrichosis is an increase in vellus Not androgen dependent (contrast with ) III. Causes Medications See Underlying disease Porphyria Congenital syndromes Hurler's Syndrome Trisomy 18 Normal states Advanced age Ethnic background Pregnancy IV. Differential Diagnosis Excessive androgen-dependent pigmented V. Management See Images: Related links to external sites (from Bing) These images

2018 FP Notebook

11. Hypertrichosis cubiti, a case report and literature review (PubMed)

Hypertrichosis cubiti, a case report and literature review Hypertrichosis cubiti is an uncommon congenital hypertrichosis with links to genetic syndromes, both autosomal dominant and recessive, with variable penetrance and expressivity. It may also present in sporadic cases with no phenotypic abnormalities or family history.

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2015 Clinical Case Reports

12. The disruption of a novel limb cis-regulatory element of SHH is associated with autosomal dominant preaxial polydactyly-hypertrichosis. (PubMed)

The disruption of a novel limb cis-regulatory element of SHH is associated with autosomal dominant preaxial polydactyly-hypertrichosis. The expression gradient of the morphogen Sonic Hedgehog (SHH) is crucial in establishing the number and the identity of the digits during anteroposterior patterning of the limb. Its anterior ectopic expression is responsible for preaxial polydactyly (PPD). Most of these malformations are due to the gain-of-function of the Zone of Polarizing Activity Regulatory (...) Sequence, the only limb-specific enhancer of SHH known to date. We report a family affected with a novel condition associating PPD and hypertrichosis of the upper back, following an autosomal dominant mode of inheritance. This phenotype is consistent with deregulation of SHH expression during limb and follicle development. In affected members, we identified a 2 kb deletion located ~240 kb upstream from the SHH promoter. The deleted sequence is capable of repressing the transcriptional activity

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2015 European Journal of Human Genetics

13. Congenital Generalized Hypertrichosis, Gingival Hyperplasia, a Coarse Facies with Constriction Bands: A Rare Association (PubMed)

Congenital Generalized Hypertrichosis, Gingival Hyperplasia, a Coarse Facies with Constriction Bands: A Rare Association Congenital generalized hypertrichosis terminalis is a rare primary hypertrichotic condition, of unknown etiology presenting in the pediatric population. Though benign in nature, there is considerable psychosocial trauma attached to this, owing to the cosmetic disfigurement it produces. The association of gingival fibromatosis and a coarse facies could further worsen

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2015 International journal of trichology

14. H Syndrome; a Multifaceted Histiocytic Disorder with Hyperpigmentation and Hypertrichosis. (PubMed)

H Syndrome; a Multifaceted Histiocytic Disorder with Hyperpigmentation and Hypertrichosis. 26015165 2016 08 12 2015 11 04 1651-2057 95 8 2015 Nov Acta dermato-venereologica Acta Derm. Venereol. H syndrome: a multifaceted histiocytic disorder with hyperpigmentation and hypertrichosis. 1021-3 10.2340/00015555-2145 Tekin Burak B Department of Dermatology, Marmara University School of Medicine, 34899 Istanbul, Turkey. burak.tekin@marmara.edu.tr. Atay Zeynep Z Ergun Tulin T Can Meryem M Tuney Davut (...) D Babay Sofia S Turan Serap S Bereket Abdullah A Zlotogorski Abraham A Molho-Pessach Vered V eng Case Reports Journal Article Sweden Acta Derm Venereol 0370310 0001-5555 0 Nucleoside Transport Proteins 0 SLC29A3 protein, human IM Adult Child Hearing Loss, Sensorineural genetics Histiocytes pathology Humans Hyperpigmentation genetics pathology Hypertrichosis genetics pathology Male Nucleoside Transport Proteins genetics Phenotype Syndrome 2015 5 28 6 0 2015 5 28 6 0 2016 8 16 6 0 ppublish

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2015 Acta Dermato-Venereologica

15. Congenital Hypertrichosis Lanuginosa (Follow-up)

Congenital Hypertrichosis Lanuginosa (Follow-up) Congenital Hypertrichosis Lanuginosa Treatment & Management: Medical Care, Surgical Care, Consultations Edition: No Results No Results Please confirm that you would like to log out of Medscape. If you log out, you will be required to enter your username and password the next time you visit. https://profreg.medscape.com/px/getpracticeprofile.do?method=getProfessionalProfile&urlCache (...) =aHR0cHM6Ly9lbWVkaWNpbmUubWVkc2NhcGUuY29tL2FydGljbGUvMTA3Mjk4Ny10cmVhdG1lbnQ= processing > Congenital Hypertrichosis Lanuginosa Treatment & Management Updated: Aug 28, 2018 Author: Dirk M Elston, MD; Chief Editor: William D James, MD Share Email Print Feedback Close Sections Sections Congenital Hypertrichosis Lanuginosa Treatment Medical Care The use of eflornithine (Vaniqa cream) 13.9% or hair removal by means of repeated shaving, depilatory methods (eg, chemical, electric methods), or bleaching can improve congenital hypertrichosis lanuginosa (CHL) patients

2014 eMedicine.com

16. Congenital Hypertrichosis Lanuginosa (Diagnosis)

Congenital Hypertrichosis Lanuginosa (Diagnosis) Congenital Hypertrichosis Lanuginosa: Background, Pathophysiology, Etiology Edition: No Results No Results Please confirm that you would like to log out of Medscape. If you log out, you will be required to enter your username and password the next time you visit. https://profreg.medscape.com/px/getpracticeprofile.do?method=getProfessionalProfile&urlCache=aHR0cHM6Ly9lbWVkaWNpbmUubWVkc2NhcGUuY29tL2FydGljbGUvMTA3Mjk4Ny1vdmVydmlldw== processing (...) > Congenital Hypertrichosis Lanuginosa Updated: Aug 28, 2018 Author: Dirk M Elston, MD; Chief Editor: William D James, MD Share Email Print Feedback Close Sections Sections Congenital Hypertrichosis Lanuginosa Overview Background For hundreds of years, societies have maintained a certain fascination with the bizarre and the unknown. In the past, persons with congenital disorders that cause excessive body-hair growth have been so dramatized and romanticized that individuals with rare hypertrichosis

2014 eMedicine.com

17. Congenital Hypertrichosis Lanuginosa (Treatment)

Congenital Hypertrichosis Lanuginosa (Treatment) Congenital Hypertrichosis Lanuginosa Treatment & Management: Medical Care, Surgical Care, Consultations Edition: No Results No Results Please confirm that you would like to log out of Medscape. If you log out, you will be required to enter your username and password the next time you visit. https://profreg.medscape.com/px/getpracticeprofile.do?method=getProfessionalProfile&urlCache (...) =aHR0cHM6Ly9lbWVkaWNpbmUubWVkc2NhcGUuY29tL2FydGljbGUvMTA3Mjk4Ny10cmVhdG1lbnQ= processing > Congenital Hypertrichosis Lanuginosa Treatment & Management Updated: Aug 28, 2018 Author: Dirk M Elston, MD; Chief Editor: William D James, MD Share Email Print Feedback Close Sections Sections Congenital Hypertrichosis Lanuginosa Treatment Medical Care The use of eflornithine (Vaniqa cream) 13.9% or hair removal by means of repeated shaving, depilatory methods (eg, chemical, electric methods), or bleaching can improve congenital hypertrichosis lanuginosa (CHL) patients

2014 eMedicine.com

18. Congenital Hypertrichosis Lanuginosa (Overview)

Congenital Hypertrichosis Lanuginosa (Overview) Congenital Hypertrichosis Lanuginosa: Background, Pathophysiology, Etiology Edition: No Results No Results Please confirm that you would like to log out of Medscape. If you log out, you will be required to enter your username and password the next time you visit. https://profreg.medscape.com/px/getpracticeprofile.do?method=getProfessionalProfile&urlCache=aHR0cHM6Ly9lbWVkaWNpbmUubWVkc2NhcGUuY29tL2FydGljbGUvMTA3Mjk4Ny1vdmVydmlldw== processing (...) > Congenital Hypertrichosis Lanuginosa Updated: Aug 28, 2018 Author: Dirk M Elston, MD; Chief Editor: William D James, MD Share Email Print Feedback Close Sections Sections Congenital Hypertrichosis Lanuginosa Overview Background For hundreds of years, societies have maintained a certain fascination with the bizarre and the unknown. In the past, persons with congenital disorders that cause excessive body-hair growth have been so dramatized and romanticized that individuals with rare hypertrichosis

2014 eMedicine.com

19. Hypomelanosis of Ito and multiple naevoid hypertrichosis: Rare cutaneous mosaicism. (PubMed)

Hypomelanosis of Ito and multiple naevoid hypertrichosis: Rare cutaneous mosaicism. Hypomelanosis of Ito and naevoid hypertrichosis are both uncommon disorders and their coexistence in the same patient is rarely described. Most previously reported patients, in addition to cutaneous lesions, had multiple neurological, musculoskeletal and other organ system involvements. We present the case of a 3-year-old girl with these two naevoid disorders at sites completely exclusive of each other

2013 Australasian Journal of Dermatology

20. Localized Acquired Hypertrichosis Associated with the Application of a Splint (PubMed)

Localized Acquired Hypertrichosis Associated with the Application of a Splint We describe a 16-year-old boy whose left forearm and hand were cut by a piece of glass from a broken window as a result of the fall. He had surgical repair of his left extensor pollicis brevis, abductor pollicis brevis, and dorsal branch of the left radial nerve. Following the surgery, he was put on a splint so as to immobilize the left forearm and wrist. On removal of the splint 4 weeks post surgery, he was noticed (...) to have more hair growth on his left forearm and hand than his right counterparts. The patient was reassessed 2, 4, and 8 months after the removal of the splint. The hypertrichosis got better with time. At the last visit, the hair growth in the left forearm and hand was back to normal. Our patient represents the first reported case of localized acquired hypertrichosis following the application of a splint in the pediatric literature.

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2012 Case reports in pediatrics

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