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. 2024 Jul 1;27(4):455-457.
doi: 10.4103/aian.aian_108_24. Epub 2024 Aug 8.

Genetic Analysis of De Novo Variants in KMT2A mixed-lineage leukemia Identified in a Family of Wiedermann-Steiner Syndromes

Min Cao  1 , Tang Dan  2 , Xiaocheng Nie  3 , Biao Tang  3 , Lan Zeng  4 , Guanghuan Pi  2 , Ai Chen  2 , Hongquan Luo  5 , Shuyao Zhu  2
Affiliations

Genetic Analysis of De Novo Variants in KMT2A mixed-lineage leukemia Identified in a Family of Wiedermann-Steiner Syndromes

Min Cao et al. Ann Indian Acad Neurol. .
No abstract available

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Conflict of interest statement

There are no conflicts of interest.

Figures

Figure 1
Figure 1
Clinical photographs showing dysmorphic features of the proband and her mother. (a) The proband exhibited characteristic features such as thick eyebrows, long eyelashes, and short palpebral fissure. (b) Clinodactyly of the fifth finger. (c) Sacral dimple. (d) The proband’s mother exhibited characteristic features such as flat face
Figure 2
Figure 2
(a) Pedigrees of WDSTS. (b) Sanger sequencing chromatograms of KMT2A in the proband’s mother. (c) Sanger sequencing chromatograms of KMT2A in the proband. WDSTS = Wiedemann–Steiner syndrome
See this image and copyright information in PMC

References

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