{Reference Type}: Journal Article
{Title}: Kindler syndrome: a rare case report from Syria.
{Author}: Edrees S;Jarkas N;Hraib M;Al-Yousef K;Baddour R;
{Journal}: Ann Med Surg (Lond)
{Volume}: 85
{Issue}: 5
{Year}: 2023 May
暂无{DOI}: 10.1097/MS9.0000000000000503
{Abstract}: Kindler syndrome is a rare autosomal recessive inherited disease. The authors report a case with unique presentation that has never reported before in the medical Literatur" lanugo hair". This is a case of a 13-year-old Syrian child, who presented with difuse fine face hair, and serious urinary complications. Kindler syndrome is characterized by acral skin blistering beginning at birth, diffuse cutaneous atrophy, photosensitivity, poikiloderma, and various mucosal findings. Highlighting a set of clinical diagnostic criteria; which is used only if a genetic test is not available.