Congenital hypopituitarism is characterized by multiple pituitary hormone deficiency, including somatotroph, thyrotroph, lactotroph, corticotroph or gonadotroph deficiencies, due to mutations of pituitary transcription factors involved in pituitary ontogenesis.
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Pallister-Hall syndrome
MONDO:0007804
non-acquired combined pituitary hormone deficiency with spine abnormalities
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short stature-pituitary and cerebellar defects-small sella turcica syndrome
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isolated thyroid-stimulating hormone deficiency
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ANE syndrome
MONDO:0012794
postaxial polydactyly-anterior pituitary anomalies-facial dysmorphism syndrome
MONDO:0014369