Three Case Reports of 22q11.2 Deletion Syndrome (CATCH22)

Three Case Reports of Esophageal Tuberculosis

Rare cases of esophageal tuberculosis have been reported. In this report, 3 cases of tuberculosis-resulted ulcer in the esophageal mucosa are to be introduced among 29 cases of gastrointestinal tuberculosis. The first patient was presented with chills and fever and had a mild dysphagia and odynnophagia and a burning sensation behind the sternum. The second case admitted with neck fistula and e...

Otodental syndrome: three familial case reports.

Guillain Barre syndrome. Three case reports.

Guillain Barre Syndrome (GBS), was originally described by Guillain et. al in 1916 following two case reports. In 1936 Guillain himself described more cases in a further report} and since then this condition has been widely published. Several different terms have been used to describe this illness and these includes acute infective polyneuritis, acute febrile polyneuritis of OsIer and acute idi...

A Case of CATCH22 Syndrome Diagnosed in Postmenopausal Woman

CATCH 22 Syndrome is caused by chromosome 22q11.2 microdeletion, characterized by developmental abnormalities of the third and fourth pharyngeal pouches. It has a prevalence estimated at 1:3,000-1:9,000. Most deletions occurs sporadic, but autosomal dominant inheritance observed in 6-10% of cases. CATCH22 often diagnosed due to hypocalcemia during neonatal period or decreased immunity or facial...

Kindler Syndrome: 2 Case Reports from India

Kindler syndrome (KS) is a rare autosomal recessive genodermatosis. We report two cases of KS with classical clinical presentations involving skin and mucus membranes. Clinically, both patients had four major features of KS in the form of acral skin blistering, photosensitivity, progressive poikiloderma, and diffuse cutaneous atrophy. Case 1 had associated features in the form of urethral...