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Items: 3

1.

Pigmented nodular adrenocortical disease, primary, 4

Cushing syndrome is a clinical designation for the systemic signs and symptoms arising from excess cortisol production. Affected individuals typically show hypertension, impaired glucose tolerance, central obesity, osteoporosis, and sometimes depression. Corticotropin-independent Cushing syndrome results from autonomous cortisol production by the adrenal glands, often associated with adrenocortical tumors. Adrenocortical tumors are most common in adult females (summary by Cao et al., 2014; Sato et al., 2014). [from OMIM]

MedGen UID:
862862
Concept ID:
C4014425
Disease or Syndrome
2.

Tessadori-Van Haaften neurodevelopmental syndrome 3

Tessadori-Bicknell-van Haaften neurodevelopmental syndrome-3 (TEBIVANED3) is characterized by global developmental delay with poor overall growth, impaired intellectual development, and speech difficulties. More variable features include hypotonia, microcephaly, and dysmorphic facies. The severity and manifestations of the disorder are highly variable (Tessadori et al., 2022). For a discussion of genetic heterogeneity of Tessadori-Bicknell-van Haaften neurodevelopmental disorder, see TEBIVANED1 (619758). [from OMIM]

MedGen UID:
1824083
Concept ID:
C5774310
Disease or Syndrome
3.

Moon facies

A rounded, puffy face with fat deposits in the temporal fossa and cheeks, a double chin. [from HPO]

MedGen UID:
568451
Concept ID:
C0332601
Sign or Symptom
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