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Items: 2

1.

Arrhinia with choanal atresia and microphthalmia syndrome

Bosma arhinia microphthalmia syndrome (BAMS) is characterized by severe hypoplasia of the nose and eyes, palatal abnormalities, deficient taste and smell, inguinal hernias, hypogonadotropic hypogonadism with cryptorchidism, and normal intelligence (summary by Graham and Lee, 2006). Also see absence of nasal bones (161480). [from OMIM]

MedGen UID:
355084
Concept ID:
C1863878
Disease or Syndrome
2.

Facioscapulohumeral muscular dystrophy 2

Facioscapulohumeral muscular dystrophy (FSHD) typically presents with weakness of the facial muscles, the stabilizers of the scapula, or the dorsiflexors of the foot. Severity is highly variable. Weakness is slowly progressive and approximately 20% of affected individuals eventually require a wheelchair. Life expectancy is not shortened. [from GeneReviews]

MedGen UID:
320405
Concept ID:
C1834671
Disease or Syndrome

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