De Morsier-Gauthier syndrome

Introduction: De Morsier-Gauthier syndrome

Description of De Morsier-Gauthier syndrome

De Morsier-Gauthier syndrome: A syndrome, sometimes considered as three separate entities (Kalmann syndromes 1, 2, and 3), characterized mainly by reduced hypothalamic function and reduced pituitary gonadotropic activity and deficiency of gonadotropin-releasing hormone with resulting hypogonadism and absent or reduced sense of smell due to agenesis of the olfactory bulbs. Associated anomalies include cleft palate, neurosensory hearing loss, congenital heart defect, intestinal malrotation, renal agenesis, hypertension, mental retardation, color blindness, and other defects. Most abnormalities occur in types 1 and 2; type 3 is marked mainly by hypogonadotropic hypogonadism, anosmia, and craniofacial abnormalities.
Source: Diseases Database

De Morsier-Gauthier syndrome: Related Topics

These medical condition or symptom topics may be relevant to medical information for De Morsier-Gauthier syndrome:

• De Morsier

Terms associated with De Morsier-Gauthier syndrome:

Terms Similar to De Morsier-Gauthier syndrome:

• Kallmann syndrome
• Olfactogenital dysplasia

Source: Diseases Database

External links related to: De Morsier-Gauthier syndrome

• Search Jablonski's Syndromes Database
• OMIM - KALLMANN SYNDROME 2; KAL2
• eMedicine - Kallmann Syndrome and Idiopathic Hypogonadotropic Hypogonadism : Article by Nicholas A Tritos, MD, DSc, FACE, FACP
• OMIM - KALLMANN SYNDROME 3; KAL3
• Kallmann's syndrome (www.whonamedit.com)
• OMIM - KALLMANN SYNDROME 1; KAL1

Source: Diseases Database

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