Farheen Khan

Family Medicine
2727 W Holcombe Blvd
Houston, TX 77025

Last Updated: 09/26/2026

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Found 8 publications

Recurrent Kawasaki Disease in a Three-Year-Old Boy: A Case Report and Review of the Literature.

Recurrent Kawasaki Disease in a Three-Year-Old Boy: A Case Report and Review of the Literature.

Journal: Cureus
Published: December 03, 2025

Left-Sided Diaphragmatic Hernia Following Pediatric Liver Transplantation: First Reported Case From the Middle East.

Left-Sided Diaphragmatic Hernia Following Pediatric Liver Transplantation: First Reported Case From the Middle East.

Journal: Cureus
Published: November 15, 2025

A Rare Case of Pediatric Infective Endocarditis Initially Presenting as Meningitis in a Previously Healthy Child.

A Rare Case of Pediatric Infective Endocarditis Initially Presenting as Meningitis in a Previously Healthy Child.

Journal: Cureus
Published: July 10, 2025

Defying the Odds: A Case Report of ACTG2-Related Megacystis-Microcolon-Intestinal Hypoperistalsis Syndrome With Complete Recovery.

Defying the Odds: A Case Report of ACTG2-Related Megacystis-Microcolon-Intestinal Hypoperistalsis Syndrome With Complete Recovery.

Journal: Cureus
Published: May 19, 2025

Characterization of a 16-Year-Old Long-Time Survivor of Edwards Syndrome.

Characterization of a 16-Year-Old Long-Time Survivor of Edwards Syndrome.

Journal: Cureus
Published: June 28, 2021

Acute Bilateral Femoral Arterial Thrombosis in a Young Adult: A Rare Association With Asymptomatic COVID-19.

Acute Bilateral Femoral Arterial Thrombosis in a Young Adult: A Rare Association With Asymptomatic COVID-19.

Journal: Cureus
Published: May 31, 2021

Optic Neuritis in a Child With COVID-19: A Rare Association.

Optic Neuritis in a Child With COVID-19: A Rare Association.

Journal: Cureus
Published: April 30, 2021

Clinical and Biochemical Features in a Case of Familial Hypocalciuric Hypercalcemia Type 3 with AP2S1 Gene Mutation in Codon Arg15His.

Clinical and Biochemical Features in a Case of Familial Hypocalciuric Hypercalcemia Type 3 with AP2S1 Gene Mutation in Codon Arg15His.

Journal: Case reports in pediatrics
Published: August 21, 2019
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Last Updated: 09/26/2026