Evidence map›Paper›PMID 39669041›Full record

ArticleJournal of orthopaedic case reports2024

Idiopathic Developmental Dysplasia of Hip in a Female Child with a Rare Epidermal Syndrome- A Case Report.

Eshaan Mishra, Nirmal C Mohapatra, Rajesh Rana, Soumitesh S Das, Chandrakanta Mishra

Abstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Journal of orthopaedic case reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

5 authors.

Eshaan MishraDepartment of Orthopaedics, SCB Medical College and Hospital, Cuttack, Odisha, India.
Nirmal C MohapatraDepartment of Orthopaedics, SCB Medical College and Hospital, Cuttack, Odisha, India.
Rajesh RanaDepartment of Orthopaedics, SCB Medical College and Hospital, Cuttack, Odisha, India.
Soumitesh S DasDepartment of Orthopaedics, SCB Medical College and Hospital, Cuttack, Odisha, India.
Chandrakanta MishraDepartment of Cardiology, SCB Medical College and Hospital, Cuttack, Odisha, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Developmental dysplasia of the hip (DDH) describes a spectrum of disorders affecting the neonatal hip. Trachyonychia or twenty nail dystrophy refers to thin, brittle nails with excessive longitudinal ridging affecting all twenty nails. Alopecia universalis congenita (ALUNC) is a rare anomaly affecting skin and appendages. It shows a genetic preponderance with its autosomal recessive variety being the most common and severe variety. Case Report: We report a case showing idiopathic DDH in a female child with a rare epidermal syndrome consisting of Trachyonychia and ALUNC. The cutaneous symptoms show familial inheritance in the form of autosomal dominant inheritance. Conclusion: This case report highlights the fact that DDH can be associated with other syndromes which require multidisciplinary evaluation and research.

Indexed as

alopecia universalis congenitaautosomal dominant inheritanceDevelopmental dysplasia of the hipTrachyonychia

Identifiers

PMID39669041
PMCPMC11632497

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