Talk:Pyruvate dehydrogenase deficiency

Epilepsy High‑importance

	This article is within the scope of WikiProject Epilepsy, a collaborative effort to improve the coverage of epilepsy and epileptic seizures on Wikipedia. If you would like to participate, please visit the project page, where you can join the discussion and see a list of open tasks.EpilepsyWikipedia:WikiProject EpilepsyTemplate:WikiProject EpilepsyEpilepsy articles
High	This article has been rated as High-importance on the project's importance scale.

Medicine: Genetics / Neurology Low‑importance

	Medicine portal This article is within the scope of WikiProject Medicine, which recommends that medicine-related articles follow the Manual of Style for medicine-related articles and that biomedical information in any article use high-quality medical sources. Please visit the project page for details or ask questions at Wikipedia talk:WikiProject Medicine.MedicineWikipedia:WikiProject MedicineTemplate:WikiProject Medicinemedicine articles
Low	This article has been rated as Low-importance on the project's importance scale.
	This article is supported by the Medical genetics task force (assessed as High-importance).
	This article is supported by the Neurology task force (assessed as High-importance).

Molecular Biology: Genetics

	This article is within the scope of WikiProject Molecular Biology, a collaborative effort to improve the coverage of Molecular Biology on Wikipedia. If you would like to participate, please visit the project page, where you can join the discussion and see a list of open tasks.Molecular BiologyWikipedia:WikiProject Molecular BiologyTemplate:WikiProject Molecular BiologyMolecular Biology articles
???	This article has not yet received a rating on the importance scale.
	This article is supported by the Genetics task force (assessed as Low-importance).

Ideal sources for Wikipedia's health content are defined in the guideline Wikipedia:Identifying reliable sources (medicine) and are typically review articles. Here are links to possibly useful sources of information about Pyruvate dehydrogenase deficiency.

PubMed provides review articles from the past five years (limit to free review articles)
The TRIP database provides clinical publications about evidence-based medicine.
Other potential sources include: Centre for Reviews and Dissemination and CDC

X-Linked Disease edit

During my studies currently, I have come across multiple sources citing different hereditary patterns. Many say X-Linked Dominant while others say X-Linked Recessive. I was wondering if anyone can shed some light on this discrepancy. The sources saying X-Linked recessive are online sources such as AMBOSS and a resource for the USMLE Step 1 exam; Pixorize. The source saying it is X-Linked Dominant are my textbooks sourced below.

Mark's Basic Medical Biochemistry ^[1]

Lippincott's Illustrated Reviews ^[2]

References

^ Marks' basic medical biochemistry : a clinical approach (Fourth edition ed.). Wolters Kluwer Health/Lippincott Williams & Wilkins. p. 369. ISBN 978-1-60831-572-7. {{cite book}}: |edition= has extra text (help)
^ Biochemistry (6th ed.). Wolters Kluwer Health/Lippincott Williams & Wilkins. p. 111. ISBN 978-1-4511-7562-2.

Add topic

[1] Marks' basic medical biochemistry : a clinical approach (Fourth edition ed.). Wolters Kluwer Health/Lippincott Williams & Wilkins. p. 369. ISBN 978-1-60831-572-7. {{cite book}}: |edition= has extra text (help)

[2] Biochemistry (6th ed.). Wolters Kluwer Health/Lippincott Williams & Wilkins. p. 111. ISBN 978-1-4511-7562-2.

[1]

[2]