Singleton‐Merten syndrome: A rare cause of femoral head necrosis-Reference-Cited by-同舟云学术

Singleton‐Merten syndrome: A rare cause of femoral head necrosis

Published:2021-06-30 Issue:10 Volume:185 Page:3170-3175
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am J Med Genet

Author:

Assaf Elio¹^ORCID,Bdeir Mohamad¹,Mohs Elisabeth¹,Dally Franz‐Joseph¹,Gravius Sascha¹,Weis Cleo‐Aron²,Darwich Ali¹

Affiliation:

1. Department of Orthopedics and Trauma Surgery University Medical Centre, Medical Faculty Mannheim of the University of Heidelberg Mannheim Germany

2. Institute of Pathology University Medical Centre, Medical Faculty Mannheim of the University of Heidelberg Mannheim Germany

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.62395

Reference19 articles.

1. S3 guideline. Part 1: Diagnosis and differential diagnosis of non‐traumatic adult femoral head necrosis;Bohndorf K.;Zeitschrift für Orthopädie und Unfallchirurgie,2015

2. Unusual cutaneous features associated with a heterozygous gain-of-function mutation inIFIH1: overlap between Aicardi-Goutières and Singleton-Merten syndromes

3. Cole Disease Results from Mutations in ENPP1

4. Singleton-Merten syndrome: An autosomal dominant disorder with variable expression

5. Mutations in DDX58, which Encodes RIG-I, Cause Atypical Singleton-Merten Syndrome

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1. Early-Age Manifestation of Singleton Merten Syndrome With Systemic Lupus Erythematosus Features: A Case Report;Cureus;2022-05-23