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23 Possible Causes for Asymmetric Nipples, Hypertelorism, Short Neck

  • Noonan Syndrome

    Noonan syndrome is an autosomal, dominantly inherited disease; it is physically characterized by short stature, short neck, webbed neck, abnormal auricles, high arched palate[] Craniofacial anomalies in affected patients include hypertelorism and severe open bite associated with masticatory dysfunction.[] In addition, nipples were wide-spaced and appeared to be low-set. On genital examination, testicles appeared to be small.[]

  • Craniofrontonasal Dysplasia

    neck Short stature Split nail Telecanthus Toe syndactyly Umbilical hernia Unilateral breast hypoplasia Wide nasal bridge Widow's peak X-linked dominant inheritance Last updated[] Nine patients had surgery for hypertelorism. The preferred technique for hypertelorism correction was facial bipartition.[] nipples and volume, webbed neck, hand or foot abnormalities such as clinodactyly (most common is a curved 5th finger) and cutaneous syndactyly (webbed fingers / toes).Females[]

  • Frontonasal Dysplasia

    neck, relatively long trunk with short limbs; cryptorchidism; and polydactyly of hands and feet.[] A general discussion of ocular hypertelorism and dystopia canthorum is presented. Ocular hypertelorism is considered a sign which may occur in a variety of disorders.[] A low implantation of the breasts was seen in the majority of patients (19/21), and in addition most of them had asymmetrical heights of their nipples (11/19).[]

  • Trisomy 4p

    […] asymmetric eyes, small ears, a short neck, finger/toe abnormalities, and behavioral problems.[] This paper describes a 2 year-old female child with the characteristic findings of frontal bossing, deep-set eyes, broad nasal bridge giving the appearance of hypertelorism[] He had an asymmetrical cry, wide spread nipples, rocker bottom feet, and clenched hands (with camptodactyly curled fingers) just to name a few of the obvious signs we were[]

  • Malpuech Syndrome

    ]; Short neck; Webbed neck CARDIOVASCULAR: [Heart]; Atrial septal defect (less common); [Vascular]; Patent ductus arteriosus (less common) CHEST: [External features]; Widely[] Malpuech syndrome shows IUGR, hypertelorism, cleft lip and palate, micropenis, hypospadias, renal anomalies, and caudal appendage. All are autosomal recessive.[] We report on two Italian brothers with facial clefting, hypertelorism, urogenital anomalies including micropenis, shawl scrotum, hearing loss, caudal appendage, and umbilical[]

  • Bifid Nose

    Zone of the neck, shoulders, chest and back A true short and webbed neck was present in 12/18 patients and in addition a mild webbing or pseudo-webbing of the neck was present[] We report five individuals in 3 generations of a family who had a bifid nose without apparent hypertelorism or mental retardation.[] Midline facial clefts are rare deformities with a wide range of clinical findings from a simple midline vermillion notch to major skeletal malformations, including orbital hypertelorism[]

  • Congenital Aural Atresia

    Symptoms Symptoms of multiple pterygium syndrome, Escobar type vary but may include short stature, vertebral (spine) defects, joint contractures, and webbing of the neck,[] Stevenson ; Introduction ; 33.1 Amastia-Hypomastia ; 33.2 Enlarged Breasts ; 33.3 Supernumerary Nipples ; 33.4 Widely Spaced Nipples ; 33.5 Gynecomastia ; Chapter 34 Asymmetric[] The most consistent characteristics of the MMF embryopathy phenotype include cleft lip and palate, microtia and aural atresia, and ocular anomalies (hypertelorism, arching[]

  • Velocardiofacial Syndrome

    […] and crowded teeth, short broad neck and shield chest with pectus deformity and widely spaced nipples with abnormal fat distribution, heart defect, scoliosis, asymmetric limb[] […] velocardiofacial syndrome are as follows: Abnormalities of the palate like cleft palate Characteristic facial features like a narrow groove of the upper lip, wide-set eyes, hypertelorism[] Many patients present with mild facial dysmorphism (e.g. malar flatness, ptosis, hypertelorism, epicanthal folds, prominent nasal root) and vertebral anomalies (e.g. butterfly[]

  • Monosomy 1p36 Syndrome

    However, some features seen in at least one of the four reported patients were not observed in our patient, including large anterior fontanelle, brachycephaly, short neck,[] […] growth Retarded growth [ more ] 0001510 High palate Elevated palate Increased palatal height [ more ] 0000218 Hydrocephalus Too much cerebrospinal fluid in the brain 0000238 Hypertelorism[] […] individuals with SMS have distinctive facial features including a broad, square-shaped facial appearance, a prominent forehead, deep-set eyes that are farther apart than usual (hypertelorism[]

  • Ring Chromosome 19

    neck, widely spaced nipples, puffy hand and feet, dark pigmented naevi, caf -au-lait spots, microcephaly, growth delay, speech delay, severe intellectual impairment, seizures[] […] infant evaluated for severe hypotonia, psychomotor retardation, and facial dysmorphisms, including round face, high prominent forehead, downward slanted palpebral fissures, hypertelorism[] […] and dysmorphic ears with prominent helix, spaced nipples, and tapering fingers (Fig. 1).[]

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