Borjeson-Forssman-Lehmann syndrome

Bör·je·son-Forss·man-Leh·mann syn·drome

(bōr'yĕ-sŏn fōrs'măn lā'mahn), [MIM*301900] a condition characterized by mental deficiency, epilepsy, hypogonadism, hypometabolism, obesity, large ears, and narrow palpebral fissures; X-linked recessive inheritance.

Börjeson,

Mats, Swedish physician, 1922–. Börjeson-Forssman-Lehmann syndrome - a condition characterized by mental deficiency, epilepsy, hypogonadism, hypometabolism, obesity, and narrow palpebral fissures.

Forssman,

Hans, Swedish physician, 1912–. Börjeson-Forssman-Lehmann syndrome - see under Börjeson

Lehmann,

J.O. Orla, Swedish pathologist, 1927–. Börjeson-Forssman-Lehmann syndrome - see under Börjeson

单词	borjeson-forssman-lehmann syndrome
释义	Borjeson-Forssman-Lehmann syndrome Bör·je·son-Forss·man-Leh·mann syn·drome (bōr'yĕ-sŏn fōrs'măn lā'mahn), [MIM301900] a condition characterized by mental deficiency, epilepsy, hypogonadism, hypometabolism, obesity, large ears, and narrow palpebral fissures; X-linked recessive inheritance. Börjeson, Mats, Swedish physician, 1922–. Börjeson-Forssman-Lehmann syndrome* - a condition characterized by mental deficiency, epilepsy, hypogonadism, hypometabolism, obesity, and narrow palpebral fissures. Forssman, Hans, Swedish physician, 1912–. Börjeson-Forssman-Lehmann syndrome - see under Börjeson Lehmann, J.O. Orla, Swedish pathologist, 1927–. Börjeson-Forssman-Lehmann syndrome - see under Börjeson AcronymsSeeBFLS
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