Non-Acquired Combined Pituitary Hormone Deficiency
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.
Známé také jako
congenital combined pituitary hormone deficiency; congenital hypopituitarism
Zahrnuje 28 příbuzných podtypů ↓Skrýt podtypy ↑
- alobar holoprosencephaly
- ANE syndrome
- chromosome 1q41-q42 deletion syndrome
- congenital hypothalamic hamartoma syndrome
- deficiency in anterior pituitary function - variable immunodeficiency syndrome
- holoprosencephaly
- holoprosencephaly 1
- holoprosencephaly 10
- holoprosencephaly 11
- holoprosencephaly 12 with or without pancreatic agenesis
- holoprosencephaly 13, X-linked
- holoprosencephaly 14
- holoprosencephaly 2
- holoprosencephaly 3
- holoprosencephaly 4
- holoprosencephaly 5
- holoprosencephaly 6
- holoprosencephaly 7
- holoprosencephaly 8
- holoprosencephaly 9
- lobar holoprosencephaly
- microform holoprosencephaly
- non-acquired combined pituitary hormone deficiency with spine abnormalities
- Pallister-Hall syndrome
- postaxial polydactyly-anterior pituitary anomalies-facial dysmorphism syndrome
- semilobar holoprosencephaly
- short stature-pituitary and cerebellar defects-small sella turcica syndrome
- solitary median maxillary central incisor syndrome
