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Items: 7

1.

Lateral meningocele syndrome

NOTCH3-related lateral meningocele syndrome (LMS) is characterized by multiple lateral spinal meningoceles (protrusions of the arachnoid and dura through spinal foramina), distinctive facial features, joint hyperextensibility, hypotonia, and skeletal, cardiac, and urogenital anomalies. Neurologic sequelæ of the meningoceles depend on size and location and can include neurogenic bladder, paresthesia, back pain, and/or paraparesis. Other neurologic findings can include Chiari I malformation, syringomyelia, and rarely, hydrocephalus. Additional findings of LMS include developmental delay, mixed or conductive hearing loss, and cleft palate. Skeletal abnormalities may include scoliosis, vertebral fusion, scalloping of vertebrae, and wormian bones. Infants may demonstrate feeding difficulties with poor weight gain. [from GeneReviews]

MedGen UID:
342070
Concept ID:
C1851710
Disease or Syndrome
2.

Thickened earlobes-conductive deafness syndrome

Thickened earlobes-conductive deafness syndrome is characterized by microtia with thickened ear lobes, micrognathia and conductive hearing loss due to congenital ossicular anomalies. It has been described in two families. The mode of inheritance is autosomal dominant. [from ORDO]

MedGen UID:
343676
Concept ID:
C1851896
Finding
3.

Renal-genital-middle ear anomalies

MedGen UID:
341454
Concept ID:
C1849432
Disease or Syndrome
4.

Conductive deafness-malformed external ear syndrome

A very rare, syndromic genetic deafness characterized by mild to moderate conductive hearing loss, dysmorphic pinnae and lip pits or dimples. The pinnae are usually small, cup-shaped, with helix folded forward, and hearing loss is associated with malformed ossicles and displacement of the external auditory canal. [from ORDO]

MedGen UID:
347429
Concept ID:
C1857341
Disease or Syndrome
5.

Branchiogenic deafness syndrome

A multiple congenital anomalies syndrome, described in one family to date, with characteristics of branchial cysts or fistula, ear malformations, congenital hearing loss (conductive, sensorineural, and mixed), internal auditory canal hypoplasia, strabismus, trismus, abnormal fifth fingers, vitiliginous lesions, short stature and mild learning disability. Renal and urethral abnormalities are absent. [from SNOMEDCT_US]

MedGen UID:
322970
Concept ID:
C1836673
Disease or Syndrome
6.

Ossicular malformations, familial

MedGen UID:
371652
Concept ID:
C1833790
Disease or Syndrome
7.

Abnormality of the middle ear ossicles

An abnormality of the middle-ear ossicles (three small bones called malleus, incus, and stapes) that are contained within the middle ear and serve to transmit sounds from the air to the fluid-filled labyrinth (cochlea). [from HPO]

MedGen UID:
324579
Concept ID:
C1836678
Finding
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