Cover Image

Sporadic case of ichthyosis bullosa of siemens in an infant: A rare case

Saved in:

Bibliographic Details
Main Authors:	Atul Vijay (Author), Akshy Kumar (Author), Shivani Saini (Author), Shail Agarwal (Author)
Format:	Book
Published:	Wolters Kluwer Medknow Publications, 2021-01-01T00:00:00Z.
Subjects:	article
Online Access:	Connect to this object online.
Tags:	Add Tag No Tags, Be the first to tag this record!

Similar Items

A double whammy! Rare occurrence of psoriasis vulgaris in a case of X-linked recessive ichthyosis
by: Akshay Kumar Jain, et al.
Published: (2021)

Klippel-trenaunay syndrome with congenital heart disease and bony abnormalities: A rare case report
by: Shail Agarwal, et al.
Published: (2022)

A sporadic case of ichthyosis hystrix: Curth and Macklin type
by: Pragya A Nair, et al.
Published: (2017)

Christ-Siemens-Touraine syndrome: A rare case report
by: Anoop Kumar, et al.
Published: (2019)

Giant melanocytic nevus with multiple hemangiomas of the scalp and recurrent lobular capillary hemangioma
by: Atul Vijay, et al.
Published: (2022)

Christ siemens touraine syndrome: A rare case report
by: N Retnakumari, et al.
Published: (2016)

Misery of living with parthenium dermatitis: Correlation between clinical severity and quality of life
by: Shail Agarwal, et al.
Published: (2021)

Dermoscopic features of Lichenoid Pseudovesicular Papular Eruption of the Nose (LiPEN): A rare entity
by: Shivani Saini, et al.
Published: (2023)

X-linked ichthyosis along with epidermolysis bullosa
by: Shambulingappa Pallagatti, et al.
Published: (2012)

Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype-phenotype correlation
by: Mariem Ennouri, et al.
Published: (2022)

Highlights of Gene and Cell Therapy for Epidermolysis Bullosa and Ichthyosis
by: Stefanos A. Koutsoukos, et al.
Published: (2024)

Palmoplantar keratoderma in a classical case of christ-siemens-touraine syndrome: A rare association
by: Prince Yuvraj Singh, et al.
Published: (2019)

Sporadic form of epidermolysis bullosa simplex with mottled pigmentation,
by: Flávia Regina Ferreira, et al.

Christ Siemen Touraine Syndrome - A Case Report
by: A D Indurkar, et al.
Published: (2004)

Epidermolysis Bullosa in Chinese Patients: Genetic Analysis and Mutation Landscape in 57 Pedigrees and Sporadic Cases
by: Yueqian Yu, et al.
Published: (2021)

Christ-Siemens-Touraine syndrome with palmoplantar keratoderma: A rare association
by: Sunil K Kothiwala, et al.
Published: (2016)

Brunauer-Fuhs-Siemens palmoplantar keratoderma: A rare, striate type of focal palmoplantar keratoderma
by: Anup Kumar Tiwary, et al.
Published: (2016)

Christ-Siemens-Touraine Syndrome: A Case Report and Review of the Literature
by: Sepideh Mokhtari, et al.
Published: (2012)

X-linked ichthyosis presenting as erythroderma: A rare case
by: Anirban Das, et al.
Published: (2015)

A case of ichthyosis hystrix: Unusual manifestation of this rare disease
by: Projna Biswas, et al.
Published: (2014)

Oral manifestations of lamellar ichthyosis: A rare case report
by: Keerthi K Nair, et al.
Published: (2016)

A Sporadic Neonatal Case of Epidermolysis Bullosa Simplex Generalized Intermediate with KRT5 and KRT14 Gene Mutations
by: Hiroyuki Wakiguchi, et al.
Published: (2016)

Subcorneal pustular dermatosis: An unusual presentation in pediatric age group
by: Shivani Saini, et al.
Published: (2020)

Christ Siemens Touraine syndrome: Two case reports and felicitous approaches to prosthetic management
by: Navanith Renahan, et al.
Published: (2015)

Sporadic dyschromatosis universalis hereditaria: A rare case report
by: Shweta Manchanda, et al.
Published: (2017)

Harlequin ichthyosis - a rare genetic disorder : a case report
by: Ghosh Arnab, et al.
Published: (2015)

Ichthyosis Prematurity Syndrome: A Rare Form but Easily Recognizable Ichthyosis
by: Sultan Al-Khenaizan, et al.
Published: (2021)

CLINICAL AND HISTOPATHOLOGICAL CONSIDERATIONS ON THE HALLOPEAU-SIEMENS DISEASE (RDEB-HS) -A CASE REPORT
by: Cristina Popa, et al.
Published: (2018)

Epidermolysis Bullosa SimplexKoebner: A Case Report
by: Shrayash Khare, et al.
Published: (2016)

Harlequin Ichthyosis: Case Report
by: Patrícia A. Couto, et al.
Published: (2019)

Epidermolysis bullosa dystrophica inversa: case report of a novel genetic mutation, involving a rare genodermatoses
by: Abhijit S Chakraborty, et al.
Published: (2023)

Erratum: Christ Siemens Touraine syndrome: Two case reports and felicitous approaches to prosthetic management
Published: (2016)

A case of lamellar ichthyosis with rickets and carcinoma of the hypopharynx
by: Aditya Kumar Bubna, et al.
Published: (2014)

Dermoscopy deduced "neither pilus nor pores": Christ-siemens-touraine syndrome: A case report
by: Priyanka Suresh Jaju, et al.
Published: (2020)

Displasia ectodérmica hipohidrótica. Síndrome de Christ-Siemens
by: Francisco T. Hurtado García, et al.
Published: (2011)

Mosaic epidermolytic ichthyosis - case report
by: Marcela Sena Teixeira Mendes, et al.
Published: (2013)

Ichthyosis hystrix: An unusual presentation
by: Vijayeeta Jairath, et al.
Published: (2016)

Dystrophic epidermolysis bullosa: Report of a case with electron microscopic study
by: Sujatha S Reddy, et al.
Published: (2011)

Corneal perforation as a rare ocular manifestation in lamellar ichthyosis: Case report and literature review
by: Alireza Peyman, et al.
Published: (2023)

Juvenile idiopathic arthritis in infants with Harlequin Ichthyosis: two cases report and literature review
by: Cinzia Auriti, et al.
Published: (2020)