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76 Possible Causes for Almond-Shaped Eyes, Cryptorchidism, Thin Upper Lip

  • Prader-Willi Syndrome

    The clinical appearance of PWS includes dysmorphic facial features with almond-shaped eyes, a narrow bifrontal diameter, and a thin upper lip; short stature; central obesity[ncbi.nlm.nih.gov] Here we report a case of Prader-Willi syndrome, who presented at 16 years of age with diabetes mellitus and cryptorchidism.[ncbi.nlm.nih.gov] Different from western patients, the 20 Asian patients exhibited at least five of the following typical features: prominent forehead, narrow face, almond-shaped eyes, small[ncbi.nlm.nih.gov]

  • Brooks Wisniewski Brown Syndrome

    lip vermilion 0010804 Thin upper lip vermilion Thin upper lip 0000219 Triangular face Face with broad temples and narrow chin Triangular facial shape [ more ] 0000325 Percent[rarediseases.info.nih.gov] Deeply set eyes and almond shaped palpebral fissures were noted. The inner canthal distance was 2.4 cm (- 1 SD), the outer canthal distance 7.1 cm (-4 SD).[documents.tips] Almond-shaped palpebral fissure Almond shaped eyes Almond-shaped opening between the eyelids [ more ] 0007874 Bulbous nose 0000414 Cerebral atrophy Degeneration of cerebrum 0002059 Cryptorchidism[rarediseases.info.nih.gov]

  • Velocardiofacial Syndrome

    Prominent nose with narrow nasal passages Thin upper lip with a down-slanted mouth Learning disabilities in one or more areas Hearing loss Speech problems Extremes of behaviors[houghton.moneomed.com] […] optic disc • Rupture or protrusion in the groin or central abdominal region (inguinal or umbilical hernia) • Failure of the testes to descend into the scrotum in males (cryptorchidism[rarediseases.org] Typical facial features include a long face, small almond shaped eyes, a wide bridged nose, and malformations of the ear.[genedx.com]

  • Hypogonadism

    Features include emotional lability, poor gross motor skills, facial abnormalities (eg, a narrow bitemporal dimension, almond-shaped eyes, a mouth with thin upper lips and[msdmanuals.com] These observations support correction of cryptorchidism during early infancy.[ncbi.nlm.nih.gov] Clinically, CHH and KS are heterogeneous; however, in 46,XY patients, they can be characterised by under-virilisation phenotypes such as cryptorchidism and micropenis or delayed[ncbi.nlm.nih.gov]

  • Hypertelorism

    upper lip, a grooved chin, and a left preauricular cyst.[ncbi.nlm.nih.gov] The son has less striking facial features but was born with a small omphalocele, large ASD secundum, PDA, bilateral cryptorchidism right hydronephrosis, and a cystic left[ncbi.nlm.nih.gov] Prader-Willi15 (paternal) imprinting or deletionProminent nasal bridge; almond-shaped eyes; thin upper lip; short stature; obesity; small hands and feet;Hyperphagia; hypotonia[dontforgetthebubbles.com]

  • Short stature-Valvular Heart Disease-Characteristic Facies Syndrome

    upper lip, high arched palate, and a small mandible.[wwww.unboundmedicine.com] Males: cryptorchidism (70-80%), infertility.[pedclerk.bsd.uchicago.edu] Congenital neurobehavioral disorder characterized by rounded face, low forehead, almond shaped eyes, squinting, hypogonadism, hypotonia, insatiable appetite leading to obesity[icd10data.com]

  • Kallmann Syndrome Type 4

    Features include emotional lability, poor gross motor skills, facial abnormalities (eg, a narrow bitemporal dimension, almond-shaped eyes, a mouth with thin upper lips and[msdmanuals.com] They include microphallus (up to 65%), cryptorchidism (up to 73%), hearing loss ( 30%), renal agenesis, synkinesis (the involuntary movement of one hand when the other is[clinicaladvisor.com] By the age of 3, he suffered 4 surgical procedures for bilateral cryptorchidism without improvement.[umbalk.org]

  • Hypogonadotropic Hypogonadism Type 21

    Features include emotional lability, poor gross motor skills, facial abnormalities (eg, a narrow bitemporal dimension, almond-shaped eyes, a mouth with thin upper lips and[merckmanuals.com] Fertility, when desired, is achieved in most cases but cryptorchidism has a poor prognosis in males.[orpha.net] Infant boys with congenital IGD often have micropenis and cryptorchidism.[ncbi.nlm.nih.gov]

  • Kallmann Syndrome Type 3

    Features include emotional lability, poor gross motor skills, facial abnormalities (eg, a narrow bitemporal dimension, almond-shaped eyes, a mouth with thin upper lips and[msdmanuals.com] Cryptorchidism is associated with an increased risk of testicular cancers. This risk nearly doubles when cryptorchidism is bilateral.[omicsonline.org] As a rulethe penis remains infantile and the testes do not descend into the scrotum (cryptorchidism). No sexual development occurs at puberty.[medical-dictionary.thefreedictionary.com]

  • Robinow Syndrome

    upper lip vermilion Thin upper lip 0000219 Upslanted palpebral fissure Upward slanting of the opening between the eyelids 0000582 Percent of people who have these symptoms[rarediseases.info.nih.gov] […] decidual teeth, a short and upturned nose, hypertelorism, and a prominent forehead are some of the most common facial abnormalities noted, while the presence of a micropenis or cryptorchidism[symptoma.com] Congenital neurobehavioral disorder characterized by rounded face, low forehead, almond shaped eyes, squinting, hypogonadism, hypotonia, insatiable appetite leading to obesity[icd10data.com]

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