Delwedd Flaen

Pachyonychia congenita - Type 1

Wedi'i Gadw mewn:

Manylion Llyfryddiaeth
Prif Awduron:	Priyanka Sangwan (Awdur), Riti Bhatia (Awdur)
Fformat:	Llyfr
Cyhoeddwyd:	Wolters Kluwer Medknow Publications, 2023-01-01T00:00:00Z.
Pynciau:	article
Mynediad Ar-lein:	Connect to this object online.
Tagiau:	Ychwanegu Tag Dim Tagiau, Byddwch y cyntaf i dagio'r cofnod hwn!

Eitemau Tebyg

Pachyonychia congenita
gan: R Asish, et al.
Cyhoeddwyd: (2008)

Pachyonychia Congenita type 1 - A peerless entity
gan: Yugandar Inakanti, et al.
Cyhoeddwyd: (2015)

Jadassohn Lewandowsky syndrome: Type 1 pachyonychia congenita
gan: Anup Kumar Tiwary, et al.
Cyhoeddwyd: (2017)

Pachyonychia congenita Type 1: Case report and review of the literature
gan: Praveen Kumar Rathore, et al.
Cyhoeddwyd: (2016)

Pachyonychia Congenita-Associated Alopecia
gan: Azita Nikoo
Cyhoeddwyd: (2012)

Author's reply: Pachyonychia congenita Type 1: Case report and review of the literature
gan: Anupam Das
Cyhoeddwyd: (2016)

Pachyonychia congenita: A case report
gan: Silpa Ramachandran, et al.
Cyhoeddwyd: (2019)

Pachyonychia congenita: A rare genodermatosis
gan: Puneet Agarwal, et al.
Cyhoeddwyd: (2013)

Pachyonychia congenita: New classification and diagnosis
gan: Manoj Kumar Agarwala, et al.
Cyhoeddwyd: (2016)

Pachyonychia congenita: Affecting three generations!
gan: Rohit Singla, et al.
Cyhoeddwyd: (2018)

Pachyonychia congenita: Sporadic onset with mutation analysis
gan: Kavitha Athota, et al.
Cyhoeddwyd: (2023)

Pachyonychia congenita with late onset (PC tarda)
gan: A Sravanthi, et al.
Cyhoeddwyd: (2016)

Phenotype and genotype features of Vietnamese children with pachyonychia congenita
gan: Ha Thi Chu, et al.
Cyhoeddwyd: (2023)

Pachyonychia congenita tarda: A rare case report
gan: Ganapathi Moger, et al.
Cyhoeddwyd: (2013)

Pachyonychia congenita: Brief appraisal of history and current classification
gan: Naveen Kumar Kansal
Cyhoeddwyd: (2017)

Pachyonychia congenita: Report of two cases and mutation analysis
gan: Jia-Ming Yeh, et al.
Cyhoeddwyd: (2012)

Pachyonychia congenita tarda: A very rare disease entity
gan: Tasleem Arif, et al.
Cyhoeddwyd: (2017)

Keratin 17 mutations in four families from India with pachyonychia congenita
gan: Manoj Agarwala, et al.
Cyhoeddwyd: (2017)

Pachyonychia Congenita (K16) with Unusual Features and Good Response to Acitretin
gan: Fahad Almutawa, et al.
Cyhoeddwyd: (2015)

Mutation p.Arg127Pro in the 1A Domain of KRT16 Causes Pachyonychia Congenita in Chinese Patient: A Case Report of PC Associated with Acral Melanoma
gan: Ge WW, et al.
Cyhoeddwyd: (2024)

A KRT6A mutation p.Ile462Asn in a Chinese family with pachyonychia congenita, and identification of maternal mosaicism: a case report
gan: Yue Li, et al.
Cyhoeddwyd: (2021)

Skin fragility, hair abnormality and pachyonychia caused by DSP mutations:a case report and literature review
gan: Huijun WANG, et al.
Cyhoeddwyd: (2022)

Type VI Aplasia Cutis Congenita: Bart's Syndrome
gan: Ferit Kulalı, et al.
Cyhoeddwyd: (2015)

A Case of Aplasia Cutis Congenita Type VI: Bart Syndrome
gan: Yasmin Alfayez, et al.
Cyhoeddwyd: (2017)

Eruptive Syringomas on the Neck: Clinicopathological and Dermoscopic Features
gan: Gargi Taneja, et al.
Cyhoeddwyd: (2021)

Atrichia congenita
gan: Chandraprakash Chouhan, et al.
Cyhoeddwyd: (2015)

Anonychia congenita
gan: Ganesh Avhad, et al.
Cyhoeddwyd: (2012)

Sífilis congénita
gan: admin admin, et al.
Cyhoeddwyd: (2018)

Dyskeratosis congenita
gan: Lorenzo Gitto, et al.
Cyhoeddwyd: (2021)

Toxoplasmosis congénita
gan: Santiago Beltrán-Flores, et al.
Cyhoeddwyd: (2014)

Signatia congénita
gan: Clara Martínez-Tafalla López, et al.
Cyhoeddwyd: (2018)

Ichthyosis congenita, harlequin type: A case report and a brief review of literature
gan: Veeresh V Dayavannavar, et al.
Cyhoeddwyd: (2016)

Dyskeratosis congenita with DKC1 mutation: A case report
gan: Xing-Yun Zhao, et al.
Cyhoeddwyd: (2020)

Case Report: A Missense Mutation in Dyskeratosis Congenita 1 Leads to a Benign Form of Dyskeratosis Congenita Syndrome With the Mucocutaneous Triad
gan: Liqing Wang, et al.
Cyhoeddwyd: (2022)

Anoftalmía congénita bilateral
gan: Doménica Jijón, et al.
Cyhoeddwyd: (2023)

Hiperplasia adrenal congénita
gan: Janer Sepúlveda Agudelo, et al.
Cyhoeddwyd: (2001)

APLASIA CUTÁNEA CONGÉNITA
gan: Rokselys Vigo Rodríguez, et al.
Cyhoeddwyd: (2015)

Estenose esofágica congénita
gan: L. Castro, et al.
Cyhoeddwyd: (2018)

Clues to facial demodicidosis: A case illustration
gan: Vishal Gupta, et al.
Cyhoeddwyd: (2016)

Immunocompromised cutaneous district revisited: Florid scabies in paralytic limb
gan: Gargi Taneja, et al.
Cyhoeddwyd: (2021)