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Moebius-Poland syndrome and hypogonadotropic hypogonadism. 2008

Diego López de Lara, and Jaime Cruz-Rojo, and Jaime Sánchez del Pozo, and Maria Elena Gallego Gómez, and Gregorio Lledó Valera
Servicio de Endocrinologia Pediatrica, Hospital 12 de Octubre, Avda de Córdoba S/N, 28041 Madrid, Spain. dldlara@yahoo.es

UI MeSH Term Description Entries
D007006 Hypogonadism Condition resulting from deficient gonadal functions, such as GAMETOGENESIS and the production of GONADAL STEROID HORMONES. It is characterized by delay in GROWTH, germ cell maturation, and development of secondary sex characteristics. Hypogonadism can be due to a deficiency of GONADOTROPINS (hypogonadotropic hypogonadism) or due to primary gonadal failure (hypergonadotropic hypogonadism). Hypergonadotropic Hypogonadism,Hypogonadism, Isolated Hypogonadotropic,Hypogonadotropic Hypogonadism,Hypogonadism, Hypergonadotropic,Hypogonadism, Hypogonadotropic
D008297 Male Males
D011045 Poland Syndrome A syndrome which is characterized by symbrachydactyly and aplasia of the sternal head of pectoralis major. Poland Anomaly,Poland Sequence,Poland Syndactyly,Anomaly, Poland,Syndactyly, Poland,Syndrome, Poland
D003937 Diagnosis, Differential Determination of which one of two or more diseases or conditions a patient is suffering from by systematically comparing and contrasting results of diagnostic measures. Diagnoses, Differential,Differential Diagnoses,Differential Diagnosis
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000293 Adolescent A person 13 to 18 years of age. Adolescence,Youth,Adolescents,Adolescents, Female,Adolescents, Male,Teenagers,Teens,Adolescent, Female,Adolescent, Male,Female Adolescent,Female Adolescents,Male Adolescent,Male Adolescents,Teen,Teenager,Youths
D020331 Mobius Syndrome A syndrome of congenital facial paralysis, frequently associated with abducens palsy and other congenital abnormalities including lingual palsy, clubfeet, brachial disorders, cognitive deficits, and pectoral muscle defects. Pathologic findings are variable and include brain stem nuclear aplasia, facial nerve aplasia, and facial muscle aplasia, consistent with a multifactorial etiology. (Adams et al., Principles of Neurology, 6th ed, p1020) Congenital Oculofacial Paralysis, Moebius,Congenital Ophthalmoplegia and Facial Paresis,Moebius Congenital Oculofacial Paralysis,Moebius Sequence,Moebius Spectrum,Moebius Syndrome,Möbius Sequence,Mobius Syndromes,Moebius Syndromes

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