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Wyszukujesz frazę ""HYPERTRICHOSIS"" wg kryterium: Temat


Tytuł:
A recurrent KCNK4 variant in a dominant pedigree with hypertrichosis and gingival fibromatosis syndrome: Variable phenotypic expressivity and insights on patients' dental management.
Autorzy:
Elhossini RM; Clinical Genetics Department, Human Genetics and Genome Research Institute, National Research Centre, Cairo, Egypt.
Sayed IM; Orodental Genetics Department, Human Genetics and Genome Research Institute, National Research Centre, Cairo, Egypt.
Hellal US; Orodental Genetics Department, Human Genetics and Genome Research Institute, National Research Centre, Cairo, Egypt.
Mahmoud SAM; Oral & Maxillofacial Pathology Department, Faculty of Dentistry, Cairo University, Cairo, Egypt.
Aglan MS; Clinical Genetics Department, Human Genetics and Genome Research Institute, National Research Centre, Cairo, Egypt.
Hassib NF; Orodental Genetics Department, Human Genetics and Genome Research Institute, National Research Centre, Cairo, Egypt.; School of Dentistry, New Giza University, Giza, Egypt.
Abdel-Hamid MS; Medical Molecular Genetics Department, Human Genetics and Genome Research Institute, National Research Centre, Cairo, Egypt.
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Źródło:
American journal of medical genetics. Part A [Am J Med Genet A] 2024 Jan; Vol. 194 (1), pp. 39-45. Date of Electronic Publication: 2023 Sep 26.
Typ publikacji:
Journal Article
MeSH Terms:
Fibromatosis, Gingival*/diagnosis
Fibromatosis, Gingival*/genetics
Hypertrichosis*/genetics
Gingival Overgrowth*/complications
Intellectual Disability*/genetics
Intellectual Disability*/complications
Male ; Humans ; Pedigree ; Phenotype ; Syndrome ; Dental Care/adverse effects ; Potassium Channels/genetics
Czasopismo naukowe
Tytuł:
Multiple vascular anomalies and refractory pericardial effusion in a young patient with Cantu syndrome: a case report and review of the literature.
Autorzy:
Daas F; Department of Pediatrics, St. Joseph's University Medical Center, 703 Main Street, Paterson, NJ, 07503, USA. r_.
Gupta P; Department of Pediatrics Division of Genetics, St. Joseph's University Medical Center, 703 Main Street, Paterson, NJ, 07503, USA.
Kiblawi F; Department of Pediatrics Division of Cardiology, St. Joseph's University Medical Center, 703 Main Street, Paterson, NJ, 07503, USA.
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Źródło:
BMC pediatrics [BMC Pediatr] 2023 Dec 19; Vol. 23 (1), pp. 644. Date of Electronic Publication: 2023 Dec 19.
Typ publikacji:
Review; Case Reports; Journal Article
MeSH Terms:
Cardiovascular Abnormalities*
Hypertrichosis*/diagnosis
Hypertrichosis*/genetics
Hypertrichosis*/pathology
Osteochondrodysplasias*/complications
Osteochondrodysplasias*/diagnosis
Osteochondrodysplasias*/genetics
Pericardial Effusion*/diagnostic imaging
Pericardial Effusion*/etiology
Vascular Malformations*
Adolescent ; Female ; Humans ; Cardiomegaly/complications ; Cardiomegaly/genetics ; Cardiomegaly/pathology
SCR Disease Name:
Cantu syndrome
Czasopismo naukowe
Tytuł:
Juvenile Dermatomyositis With Rare Cutaneous Manifestation: Generalised Hypertrichosis.
Autorzy:
Kayani M; Department of Medicine, Medical Teaching Institute, Lady Reading Hospital, Peshawar, Pakistan.
Khalil E; Department of Medicine, Medical Teaching Institute, Lady Reading Hospital, Peshawar, Pakistan.
Sultan J; Department of Dermatology, Medical Teaching Institute, Lady Reading Hospital, Peshawar, Pakistan.
Sagheer F; Department of Dermatology, Medical Teaching Institute, Lady Reading Hospital, Peshawar, Pakistan.
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Źródło:
JPMA. The Journal of the Pakistan Medical Association [J Pak Med Assoc] 2023 Jul; Vol. 73 (7), pp. 1539-1541.
Typ publikacji:
Case Reports
MeSH Terms:
Dermatomyositis*/complications
Dermatomyositis*/diagnosis
Hypertrichosis*/diagnosis
Hypertrichosis*/etiology
Hypertrichosis*/pathology
Vascular Diseases*
Humans ; Skin/pathology ; Inflammation/pathology
Raport
Tytuł:
A child with generalized hypertrichosis due to secondary topical minoxidil exposure.
Autorzy:
Maltoni G; Pediatric Unit, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
Cedirian S; Dermatology Unit, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.; Department of Medical and Surgical Sciences, Alma Mater Studiorum University of Bologna, Bologna, Italy.
Scozzarella A; Specialty School of Pediatrics, Alma Mater Studiorum, University of Bologna, Bologna, Italy.
Bernardini L; Specialty School of Pediatrics, Alma Mater Studiorum, University of Bologna, Bologna, Italy.
Piraccini BM; Dermatology Unit, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.; Department of Medical and Surgical Sciences, Alma Mater Studiorum University of Bologna, Bologna, Italy.
Starace M; Dermatology Unit, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.; Department of Medical and Surgical Sciences, Alma Mater Studiorum University of Bologna, Bologna, Italy.
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Źródło:
Pediatric dermatology [Pediatr Dermatol] 2023 Jul-Aug; Vol. 40 (4), pp. 753-754. Date of Electronic Publication: 2023 Apr 12.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Hypertrichosis*/chemically induced
Alopecia Areata*/chemically induced
Alopecia Areata*/drug therapy
Male ; Female ; Child ; Humans ; Infant ; Minoxidil/adverse effects ; Alopecia/drug therapy ; Diazoxide/therapeutic use ; Diagnosis, Differential ; Administration, Topical
Czasopismo naukowe
Tytuł:
Localized hypertrichosis as a manifestation of contact allergy to aluminium.
Autorzy:
Xará J; Dermatology Department, Coimbra University Hospital Centre, Coimbra, Portugal.
Matos A; Dermatology Department, Coimbra University Hospital Centre, Coimbra, Portugal.
Soares J; Dermatology Department, Coimbra University Hospital Centre, Coimbra, Portugal.
Teixeira J; Dermatology Department, Coimbra University Hospital Centre, Coimbra, Portugal.
Ramos L; Dermatology Department, Coimbra University Hospital Centre, Coimbra, Portugal.; Dermatology Department, Faculty of Medicine, University of Coimbra, Coimbra, Portugal.
Gonçalo M; Dermatology Department, Coimbra University Hospital Centre, Coimbra, Portugal.; Dermatology Department, Faculty of Medicine, University of Coimbra, Coimbra, Portugal.
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Źródło:
Contact dermatitis [Contact Dermatitis] 2023 Jul; Vol. 89 (1), pp. 58-59. Date of Electronic Publication: 2023 Mar 27.
Typ publikacji:
Case Reports
MeSH Terms:
Dermatitis, Allergic Contact*/diagnosis
Dermatitis, Allergic Contact*/etiology
Hypertrichosis*/chemically induced
Humans ; Aluminum/adverse effects ; Patch Tests
Raport
Tytuł:
Cholesterol homeostasis in hair follicle keratinocytes is disrupted by impaired ABCA5 activity.
Autorzy:
Palmer MA; School of Applied Sciences, University of Huddersfield, Huddersfield, UK; Faculty of Medicine, Institute of Biochemistry I, Goethe-University Frankfurt, Frankfurt, Germany.
Dias IHK; Aston Medical school, Aston University, Birmingham, UK.
Smart E; Centre for Dermatology Research, University of Manchester, UK.
Benatzy Y; Faculty of Medicine, Institute of Biochemistry I, Goethe-University Frankfurt, Frankfurt, Germany.
Haslam IS; School of Applied Sciences, University of Huddersfield, Huddersfield, UK. Electronic address: .
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Źródło:
Biochimica et biophysica acta. Molecular and cell biology of lipids [Biochim Biophys Acta Mol Cell Biol Lipids] 2023 Sep; Vol. 1868 (9), pp. 159361. Date of Electronic Publication: 2023 Jun 20.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Hair Follicle*/metabolism
Hypertrichosis*/metabolism
Humans ; Keratinocytes/metabolism ; ATP-Binding Cassette Transporters/genetics ; ATP-Binding Cassette Transporters/metabolism ; Homeostasis ; Cholesterol/metabolism
Czasopismo naukowe
Tytuł:
Syndrome of Congenital Insulin Resistance Caused by a Novel INSR Gene Mutation
Autorzy:
Rojek A; Poznan University of Medical Sciences, Institute of Pediatrics, Department of Pediatric Endocrinology and Rheumatology, Poznan, Poland
Wikiera B; Wroclaw Medical University, Department of Endocrinology and Diabetology for Children and Adolescents, Wroclaw, Poland
Noczynska A; Wroclaw Medical University, Department of Endocrinology and Diabetology for Children and Adolescents, Wroclaw, Poland
Niedziela M; Poznan University of Medical Sciences, Institute of Pediatrics, Department of Pediatric Endocrinology and Rheumatology; Karol Jonscher’s Clinical Hospital, Poznan, Poland
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Źródło:
Journal of clinical research in pediatric endocrinology [J Clin Res Pediatr Endocrinol] 2023 Aug 23; Vol. 15 (3), pp. 312-317. Date of Electronic Publication: 2021 Dec 30.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Antigens, CD*/genetics
Cardiomyopathy, Hypertrophic*/complications
Diabetes Mellitus*
Donohue Syndrome*/diagnosis
Donohue Syndrome*/genetics
Hyperglycemia*/complications
Hypertrichosis*/complications
Hypoglycemia*/complications
Insulin Resistance*/genetics
Receptor, Insulin*/genetics
Female ; Humans ; Infant ; Infant, Newborn ; Male ; Facies ; Insulin ; Mutation
Czasopismo naukowe
Tytuł:
Low dose oral minoxidil and the conundrum of cardiovascular complications.
Autorzy:
Ibraheim MK; Department of Dermatology, Loma Linda University, Loma Linda, California, USA.
Elsensohn A
Hauschild C
Hilliard A
Dao H
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Źródło:
Dermatology online journal [Dermatol Online J] 2023 Aug 15; Vol. 29 (4). Date of Electronic Publication: 2023 Aug 15.
Typ publikacji:
Journal Article
MeSH Terms:
Minoxidil*/adverse effects
Hypertrichosis*
Humans ; Alopecia/drug therapy ; Alopecia/chemically induced ; Hair ; Antihypertensive Agents/adverse effects ; Administration, Topical
Czasopismo naukowe
Tytuł:
What's still unresolved in Hughes syndrome?
Autorzy:
Hughes G; London Lupus Centre, London Bridge Hospital, London, UK.
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Źródło:
Lupus [Lupus] 2023 Jul; Vol. 32 (8), pp. 924-927. Date of Electronic Publication: 2023 Jun 01.
Typ publikacji:
Journal Article
MeSH Terms:
Antiphospholipid Syndrome*
Lupus Erythematosus, Systemic*
Acromegaly*
Hypertrichosis*
Humans
SCR Disease Name:
Acromegaloid facial appearance syndrome
Czasopismo naukowe
Tytuł:
Overactive ATP-Sensitive K Channels Compromise Lymphatic Contractile Function in Cantú Syndrome.
Autorzy:
Aziz Q; Translational Medicine and Therapeutics, William Harvey Research Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, Charterhouse Square, London EC1M 6BQ, UK.
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Źródło:
Function (Oxford, England) [Function (Oxf)] 2023 Jun 08; Vol. 4 (4), pp. zqad030. Date of Electronic Publication: 2023 Jun 08 (Print Publication: 2023).
Typ publikacji:
Journal Article; Comment
MeSH Terms:
Cardiomegaly*
Hypertrichosis*/genetics
Humans ; Sulfonylurea Receptors ; Adenosine Triphosphate
SCR Disease Name:
Cantu syndrome
Czasopismo naukowe
Tytuł:
Anterior Cervical Hypertrichosis.
Autorzy:
Sawatkar G; Department of Dermatology Venereology and Leprology, All India Institute of Medical Sciences, Nagpur, Maharashtra.
Kowe PA; Department of Dermatology Venereology and Leprology, All India Institute of Medical Sciences, Nagpur, Maharashtra. .
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Źródło:
Indian pediatrics [Indian Pediatr] 2023 Apr 15; Vol. 60 (4), pp. 328.
Typ publikacji:
Journal Article
MeSH Terms:
Hypertrichosis*/diagnosis
Female ; Humans ; Pharynx ; Cervix Uteri
SCR Disease Name:
Hypertrichosis, anterior cervical
Czasopismo naukowe
Tytuł:
Patients with DeSanto-Shinawi syndrome: Further extension of phenotype from Italy.
Autorzy:
Pasquali D; Department of Advanced Medical and Surgical Sciences, University of Campania 'Luigi Vanvitelli', Naples, Italy.
Torella A; Genetica Medica, Department of Precision Medicine, University of Campania 'Luigi Vanvitelli', Naples, Italy.; Telethon Institute of Genetics and Medicine (TIGEM), Pozzuoli, Italy.
Grandone A; Department of Women's and Children's Health and General and Specialized Surgery, University of Campania 'Luigi Vanvitelli', Naples, Italy.
Luongo C; Department of Women's and Children's Health and General and Specialized Surgery, University of Campania 'Luigi Vanvitelli', Naples, Italy.
Morleo M; Genetica Medica, Department of Precision Medicine, University of Campania 'Luigi Vanvitelli', Naples, Italy.; Telethon Institute of Genetics and Medicine (TIGEM), Pozzuoli, Italy.
Peduto C; Genetica Medica, Department of Precision Medicine, University of Campania 'Luigi Vanvitelli', Naples, Italy.
di Fraia R; Department of Advanced Medical and Surgical Sciences, University of Campania 'Luigi Vanvitelli', Naples, Italy.
Selvaggio LD; Department of Advanced Medical and Surgical Sciences, University of Campania 'Luigi Vanvitelli', Naples, Italy.
Allosso F; Department of Advanced Medical and Surgical Sciences, University of Campania 'Luigi Vanvitelli', Naples, Italy.
Accardo G; Department of Advanced Medical and Surgical Sciences, University of Campania 'Luigi Vanvitelli', Naples, Italy.
Zanobio MT; Genetica Medica, Department of Precision Medicine, University of Campania 'Luigi Vanvitelli', Naples, Italy.
Maitz S; Pediatric Genetics Unit, MBBM Foundation, S. Gerardo Hospital, Monza, Italy.; Service of Medical Genetics, Oncologic Institute of Southern Switzerland, Lugano, Switzerland.
Mariani M; Department of Pediatrics, S. Fermo Hospital, ASST Lariana, Como, Italy.
Selicorni A; Department of Pediatrics, S. Fermo Hospital, ASST Lariana, Como, Italy.
Banfi S; Genetica Medica, Department of Precision Medicine, University of Campania 'Luigi Vanvitelli', Naples, Italy.; Telethon Institute of Genetics and Medicine (TIGEM), Pozzuoli, Italy.
Nigro V; Genetica Medica, Department of Precision Medicine, University of Campania 'Luigi Vanvitelli', Naples, Italy.; Telethon Institute of Genetics and Medicine (TIGEM), Pozzuoli, Italy.
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Corporate Authors:
TUDP Study Group
Źródło:
American journal of medical genetics. Part A [Am J Med Genet A] 2023 Mar; Vol. 191 (3), pp. 823-830. Date of Electronic Publication: 2022 Nov 24.
Typ publikacji:
Case Reports; Research Support, Non-U.S. Gov't
MeSH Terms:
Intellectual Disability*/genetics
Hypertrichosis*/genetics
Hyperandrogenism*
Humans ; Female ; Hirsutism/genetics ; Oligomenorrhea ; Phenotype
Raport
Tytuł:
Pigmented neurofibroma with hypertrichosis.
Autorzy:
Godínez-Chaparro JA; Servicio de Dermatología Pediátrica, Unidad Médica de Alta Especialidad, Hospital General Dr. Gaudencio González Garza, Centro Médico Nacional La Raza, Instituto Mexicano del Seguro Social, Mexico City.
Valencia-Herrera AM; Servicio de Dermatología del Hospital Infantil de México Federico Gómez, Mexico City.
Mena-Cedillos CA; Servicio de Dermatología del Hospital Infantil de México Federico Gómez, Mexico City.
Toussaint-Caire S; Departamento de Dermatopatología, Hospital General Dr. Manuel Gea Gónzalez, Mexico City.
Duarte-Abdala MR; Servicio de Dermatología, Hospital del Niño y del Adolescente Morelense, Morelos.
Loza-Escutia O; Hospital de Especialidades Unidad Médica de Alta Especialidad, Centro Médico La Raza, Mexico City. Mexico.
Toledo-Bahena ME; Servicio de Dermatología del Hospital Infantil de México Federico Gómez, Mexico City.
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Transliterated Title:
Neurofibroma pigmentado con hipertricosis.
Źródło:
Boletin medico del Hospital Infantil de Mexico [Bol Med Hosp Infant Mex] 2023; Vol. 80 (1), pp. 57-62.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Hypertrichosis*
Neurofibroma*
Neurofibromatosis 1*
Male ; Humans ; Child ; Melanins ; Biopsy
Czasopismo naukowe
Tytuł:
Dental anomalies in syndromes displaying hypertrichosis in the clinical spectrum.
Autorzy:
Carneiro VF; Universidade Estadual de Montes Claros - Unimontes, Primary Care Postgraduate Program, Montes Claros, MG, Brazil.
Machado RA; Universidade de São Paulo - USP, Hospital for Rehabilitation of Craniofacial Anomalies, Bauru, SP, Brazil.
Barbosa MC; Universidade Estadual de Montes Claros - Unimontes, Dental School, Department of Oral Pathology and Oral Medicine, Montes Claros, MG, Brazil.
Dias VO; Universidade Estadual de Montes Claros - Unimontes, Primary Care Postgraduate Program, Montes Claros, MG, Brazil.
Martelli DRB; Universidade Estadual de Montes Claros - Unimontes, Primary Care Postgraduate Program, Montes Claros, MG, Brazil.
Martelli-Júnior H; Universidade Estadual de Montes Claros - Unimontes, Primary Care Postgraduate Program, Montes Claros, MG, Brazil.
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Źródło:
Brazilian oral research [Braz Oral Res] 2023 Mar 31; Vol. 37, pp. e030. Date of Electronic Publication: 2023 Mar 31 (Print Publication: 2023).
Typ publikacji:
Journal Article
MeSH Terms:
Hypertrichosis*/genetics
Humans ; Phenotype
Czasopismo naukowe
Tytuł:
Crisaborole-induced acquired localized hypertrichosis in a 3-year-old male patient with atopic dermatitis.
Autorzy:
Chen M; Department of Dermatology, The Fourth School of Medicine Affiliated to Zhejiang Chinese Medical University, Zhejiang, China.
Ali K; The Fourth Affiliated Hospital of Zhejiang University, Zhejiang, China.
Shan J; Department of Dermatology, The Fourth School of Medicine Affiliated to Zhejiang Chinese Medical University, Zhejiang, China.
Xie T; Department of Dermatology, The Fourth School of Medicine Affiliated to Zhejiang Chinese Medical University, Zhejiang, China.
Wu L; Department of Dermatology, Affiliated Hangzhou First People's Hospital, Zhejiang University School of Medicine, Hangzhou, P. R. China.
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Źródło:
International journal of dermatology [Int J Dermatol] 2023 Mar; Vol. 62 (3), pp. e158-e159. Date of Electronic Publication: 2022 Nov 01.
Typ publikacji:
Letter
MeSH Terms:
Dermatitis, Atopic*
Hypertrichosis*
Male ; Humans ; Child, Preschool ; Boron Compounds ; Bridged Bicyclo Compounds, Heterocyclic ; Hirsutism ; Ointments
Opinia redakcyjna
Tytuł:
Isolated congenital nevoid linear hypertrichosis in an infant: a case report.
Autorzy:
Zimmerman L; Department of Dermatology, University of Illinois College of Medicine at Chicago, Chicago, IL, USA.
Trodello C; Department of Dermatology, University of Illinois College of Medicine at Chicago, Chicago, IL, USA.
Bain M; Department of Dermatology, University of Illinois College of Medicine at Chicago, Chicago, IL, USA.
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Źródło:
International journal of dermatology [Int J Dermatol] 2023 Feb; Vol. 62 (2), pp. e94-e95. Date of Electronic Publication: 2022 Jan 20.
Typ publikacji:
Case Reports; Letter
MeSH Terms:
Hypertrichosis*/diagnosis
Skin Neoplasms*/congenital
Nevus*
Skin Abnormalities*
Infant ; Humans
SCR Disease Name:
Congenital hypertrichosis lanuginosa
Raport
Tytuł:
Combination 1550 nm non-ablative fractional resurfacing and laser hair removal for treatment of Becker's nevi in skin types III-VI.
Autorzy:
Kubicki SL; Department of Dermatology, McGovern Medical School, University of Texas MD Anderson Cancer Center, University of Texas, Houston, Texas, USA.
Guo EL; Dermatology & Laser Surgery Center, Houston, Texas, USA.
Sodha P; Department of Dermatology, George Washington University School of Medicine and Health Sciences, Washington, District of Columbia, USA.
Richmond H; Dermatology & Laser Surgery Center, Houston, Texas, USA.
Friedman PM; Department of Dermatology, McGovern Medical School, University of Texas MD Anderson Cancer Center, University of Texas, Houston, Texas, USA.; Dermatology & Laser Surgery Center, Houston, Texas, USA.; Department of Dermatology, Weill Cornell Medical College, Houston Methodist Hospital, Houston, Texas, USA.
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Źródło:
Lasers in surgery and medicine [Lasers Surg Med] 2023 Jan; Vol. 55 (1), pp. 99-104. Date of Electronic Publication: 2022 Sep 21.
Typ publikacji:
Case Reports
MeSH Terms:
Skin Neoplasms*/radiotherapy
Skin Neoplasms*/surgery
Hair Removal*
Hypertrichosis*/complications
Hyperpigmentation*/etiology
Hyperpigmentation*/surgery
Nevus*/surgery
Nevus*/complications
Lasers, Solid-State*/therapeutic use
Humans ; Young Adult ; Adult ; Aluminum ; Neodymium ; Yttrium ; Lasers ; Treatment Outcome
Raport
Tytuł:
A Novel Variant in RAD21 in Cornelia De Lange Syndrome Type 4: Case Report and Bioinformatic Analysis.
Autorzy:
De Falco A; U.O.C. Genetica Medica, A.O.U. Federico II, 80131 Naples, Italy.; Department of Molecular Medicine and Medical Biotechnology, University Federico II, 80131 Naples, Italy.
De Brasi D; U.O.C. Pediatria, AORN Santobono Pausilipon, 80129 Naples, Italy.
Della Monica M; Medical and Laboratory Genetic Unit, Antonio Cardarelli Hospital, 80131 Naples, Italy.
Cesario C; Laboratory of Medical Genetics, Bambino Gesù Children Hospital IRCCS, 00165 Rome, Italy.
Petrocchi S; Laboratory of Medical Genetics, Bambino Gesù Children Hospital IRCCS, 00165 Rome, Italy.
Novelli A; Laboratory of Medical Genetics, Bambino Gesù Children Hospital IRCCS, 00165 Rome, Italy.
D'Alterio G; European School of Molecular Medicine, Università Degli Studi di Milano, 20139 Milan, Italy.; CEINGE Biotecnologie Avanzate, 80145 Naples, Italy.
Iolascon A; U.O.C. Genetica Medica, A.O.U. Federico II, 80131 Naples, Italy.; Department of Molecular Medicine and Medical Biotechnology, University Federico II, 80131 Naples, Italy.; CEINGE Biotecnologie Avanzate, 80145 Naples, Italy.
Capasso M; Department of Molecular Medicine and Medical Biotechnology, University Federico II, 80131 Naples, Italy.; CEINGE Biotecnologie Avanzate, 80145 Naples, Italy.
Piscopo C; Medical and Laboratory Genetic Unit, Antonio Cardarelli Hospital, 80131 Naples, Italy.
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Źródło:
Genes [Genes (Basel)] 2023 Jan 01; Vol. 14 (1). Date of Electronic Publication: 2023 Jan 01.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
De Lange Syndrome*/diagnosis
De Lange Syndrome*/genetics
Cleft Palate*
Hypertrichosis*
Female ; Humans ; Cell Cycle Proteins/genetics ; Phenotype ; DNA-Binding Proteins/genetics
Czasopismo naukowe
Tytuł:
A rare clinical image of hypertrichosis (Werewolf syndrome).
Autorzy:
Joshi T; Department of Kayachikitsa, Mahatma Gandhi Ayurveda College, Hospital and Research Centre, Salod (H), Datta Meghe Institute of Medical Sciences (DU), Sawangi, Wardha, India.
Kuchewar V; Department of Kayachikitsa, Mahatma Gandhi Ayurveda College, Hospital and Research Centre, Salod (H), Datta Meghe Institute of Medical Sciences (DU), Sawangi, Wardha, India.
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Źródło:
The Pan African medical journal [Pan Afr Med J] 2022 Oct 25; Vol. 43, pp. 99. Date of Electronic Publication: 2022 Oct 25 (Print Publication: 2022).
Typ publikacji:
Journal Article
MeSH Terms:
Hypertrichosis*/diagnosis
Humans ; Syndrome
Czasopismo naukowe

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