Hemifacial microsomia

Case contributed by Mostafa Mohamed , 13 Feb 2020
Diagnosis probable
Changed by Mostafa Mohamed, 19 Mar 2025
Disclosures - updated 15 Dec 2024: Nothing to disclose

Updates to Case Attributes

Body was changed:

Treacher-Collins syndrome is genetic  disease  characterized disease  characterised by deformities of the ears, eyes, cheekbones, and chin and sometimes affect other systems as Heart.

 It It is estimated to occur in one in 10,000 to one in 50,000 births.

Differential diagnosis include Miller syndrome and Nager syndrome but in both syndromes additional limb anomalies are seen.

Status changed from draft to published (unlisted).
Visibility changed from public to unlisted.
Published At was set to 2025-03-19T16:05:26.105Z.

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